Macrophages are one the most abundant immune cells in the TME, including in BlCa (Miyake et al., 2016; Du et al., 2021b). Tumor-associated macrophages (TAMs) secrete several soluble molecules, such as cytokines and chemokines, that directly influence tumor growth, metastasis, and drug resistance (Hanada et al., 2000; Pan et al., 2020). In BlCa, higher amounts of CD68⁺ (pan-macrophage marker) cells, were associated with higher grade and advanced tumors (Huang et al., 2020; Harras and Abo Safia, 2021). Specifically, TAMs (CD68⁺) number was significantly higher in MIBCs comparing with NMIBCs (Hanada et al., 2000; Viveiros et al., 2022) and higher amounts of CD68⁺ cells were significantly associated with poorer disease specific survival (DSS) in bladder peritumoral regions and with worse overall survival (OS) and DSS in bladder intratumoral regions (Viveiros et al., 2022). Co-cultures between macrophages and BlCa cell lines showed an increase in colony formation, cell migration and cell invasion (Huang et al., 2020). TME influence macrophage polarization and, consequently, macrophage function (Miyake et al., 2016). Macrophages can be classified in anti-tumor/proinflammatory (M1) and pro-tumor/anti-inflammatory (M2) (Miyake et al., 2016). M2 macrophages (CD163⁺) are associated with tumorigenesis, tumor growth, angiogenesis, inhibition of immunosurveillance and ECM degradation (Miyake et al., 2016; Du et al., 2021b; Harras and Abo Safia, 2021). TAMs usually display a bias towards an M2-like phenotype (Takeuchi et al., 2016), as observed in BlCa (Viveiros et al., 2022). Indeed, higher ratio of CD163⁺/CD68⁺ macrophages was correlated with advanced BlCa stage and grade (Takeuchi et al., 2016) and higher amounts of CD163+ were significantly associated with worse DSS and OS (Viveiros et al., 2022).

Fibroblasts are one of the most abundant and active cells in the stroma, performing tissue repair functions (Miyake et al., 2016). Cancer-associated fibroblasts (CAFs) contribute to tumor growth, angiogenesis and treatment resistance by secreting specific cytokines (Miyake et al., 2016). Additionally, CAFs secrete several factors, such as collagen, matrix metalloproteinases (MMPs), chemokines and proteases (Miyake et al., 2016; Du et al., 2021b). Du Y et al. demonstrated, in silico, that CAFs were abundant in bladder TME. Moreover, the authors showed that higher CAF levels enhanced BlCa progression and were associated with lower OS Du et al. (2021b). Other study demonstrated that co-culture between fibroblasts and BlCa cell lines (UMUC3, T24 and 5637) improved tumor cell invasion (Yeh et al., 2015) and have been associated with cisplatin resistance (Long et al., 2019).

Overall T cells (CD3⁺) were significant increase in MIBC tumors, comparing with high-grade NMIBCs, although no differences were found in bladder peritumoral areas (Viveiros et al., 2022). It was shown that CD3⁺ in tumor infiltrating lymphocytes (TILs) were related with poor outcome in BlCa patients (Russo et al., 2022). However, Viveiros N et al. proved that an enrichment of CD3⁺ cells, in the intratumoral area, significantly associated with higher disease-free survival (DFS) (Viveiros et al., 2022) and Sjödahl G et al. showed that infiltrating CD3⁺ cells were significantly associated with good prognosis in the MIBC cases (Sjödahl et al., 2014).

In silico, cytotoxic CD8⁺ T cells correlated with better patient outcome, being observed a decrease of CD8⁺ levels in higher BlCa stages (Cao et al., 2019; Zhang et al., 2020). In patient tissues, Zhang S et al. and Jóźwicki W et al. reported that CD8⁺ TILs was found mostly in pTa-pT1, comparing with pT2 tumors Jóźwicki et al. (2016), Zhang et al. (2017). Specifically, in Zhang S et al. study, higher CD8⁺ was associated with better OS in non-organ confined disease, but with worse OS in organ-confined disease patients, suggesting that cytotoxic T cells might have anti-tumor activity in non-organ confined disease and a pro-tumor activity in organ-confined disease Zhang et al. (2017). Viveiros N et al. observed that MIBC patients presented higher CD8⁺ expression, comparing with NMIBC high-grade, but, specifically, MIBC tumors with high intratumoral CD8 expression demonstrated higher DFS and OS Viveiros et al. (2022). Additionally, it was shown that poor CD8⁺ T cell expression, along with type I IFN signature and IFN-inducible inhibitory factors, characterize a non-T cell inflamed bladder TME (Trujillo et al., 2018), usually correlated with poor prognosis and resistance to immunotherapies (Sweis et al., 2016).

In silico, Cao J et al. observed that CD4⁺ memory resting cells decreased with higher BlCa stage, while CD4⁺ memory activated T cells increased Cao et al. (2019). Zhang Y et al. showed, in silico, that activated memory CD4⁺ cells were significantly associated with better outcome, while resting memory CD4⁺ cells were associated with poor outcome in BlCa patients Zhang et al. (2020). In BlCa tissues, CD4⁺ levels were significantly higher in pTa-pT1 patients, comparing with most aggressive tumors (Jóźwicki et al., 2016; Viveiros et al., 2022). However, stratifying the tumoral areas, it was observed that CD4⁺ cells were significantly enriched in high-grade NMIBCs in peritumoral area, while CD4⁺ levels were significantly abundant in MIBCs in intratumoral area (Viveiros et al., 2022).

Regulatory T (Treg) cells are a subpopulation of CD4⁺ T cells, characterized by the expression forkhead box protein P3 (FOXP3) transcription factor (Winerdal et al., 2011; Ariafar et al., 2020). Tregs are known to trigger several immunosuppressive mechanisms, both by contact-dependent manner, or indirectly through the secretion of several cytokines, capable of promoting tumor progression (Ariafar et al., 2020). Ariafar A et al., detected a Treg population (CD4⁺CD25+FOXP3+CD127^low/neg) in lymph nodes from BlCa patients, representing about 10% of all CD4⁺ T cells Ariafar et al. (2020). In this study, Treg cells were significantly higher in patients with at least one involved node, comparing with negative-node patients, although no impact was observed in the survival time (Ariafar et al., 2020), suggesting that Tregs might play a role in tumor metastasis formation (Ariafar et al., 2020). Viveiros N et al. observed that Treg cells were significantly lower in the peritumoral area in more advanced stages (pT3 and pT4), but were significantly higher in the intratumoral areas in pTa-pT1 (Viveiros et al., 2022). Moreover, higher Treg amounts in intratumoral areas of high-grade NMIBCs were associated with poor OS and DSS (Viveiros et al., 2022). Jóźwicki W et al. showed that Treg amounts were significantly higher in BlCa patients peripheral blood before the surgery, comparing with after surgery (Jóźwicki et al., 2016).

In BlCa, NK cells have been proved to be important in BCG-treatment (Brandau et al., 2001; Esteso et al., 2021), however less is known regarding the role of NK cells in bladder tumor immune surveillance (Sun et al., 2021a). Krpina K et al. demonstrated that NMIBC patients with recurrent disease presented significantly higher levels of stromal NK cells, compared with NMIBC patients without recurrence disease (Krpina et al., 2014). Additionally, NMIBC patients with recurrent pTa tumors, recurrent smaller tumors, and recurrent single tumors, presented significantly higher levels of stromal NK cells, than no reccurent NMIBC patients (Krpina et al., 2014). NK cells can be divided in CD56^dim NK cells (CD3⁻CD56^dimCD16⁺), presenting higher cytolytic activity, and in CD56^bright NK cells (CD3⁻CD56^brightCD16⁻), presenting immunoregulatory function through abundant cytokine production (Lin et al., 2004; Poli et al., 2009; Moretta, 2010). In BlCa patients, it was demonstrated that most NK cells were dim NK cells and the proportion of intratumoral dim NK cells were significantly higher in most advanced stages (Mukherjee et al., 2018). Furthermore, higher amounts of CD56^bright NK cells were significantly associated with better OS and cancer-specific survival (CSS) (Mukherjee et al., 2018).

DCs are specialized APCs that comprise a rare immune cell population in tumors and in lymphoid organs (Gallo and Gallucci, 2013; Wculek et al., 2020). DCs are essential in trigging antigen-specific immunity and tolerance, since present antigens to T cells and produce immunomodulatory signals by cytokines and cell-cell contacts (Wculek et al., 2020). DCs can be stratified in plasmacytoid (pDC) and in myeloid (mDC) DCs (Martin-Gayo and Yu, 2019). Although DCs are in very low amounts in peripheral blood, Rossi R et al. showed a significant decrease of mDCs and pDCs levels in NMIBC patients peripheral blood before TURBT, comparing with healthy donors (Rossi et al., 2013). Also, the authors showed a significant decrease of mDCs in low-grade NMIBC patients before TURBT, compared with high-grade NMIBC patients, while for pDCs no significant differences were observed (Rossi et al., 2013). Patients who received BCG instillations showed peripheral blood evidence of mDC recovery, especially from the third instillation until the completion of the treatment, but no appreciable alterations were detected for pDCs (Rossi et al., 2013). While urine samples did not present mDCs or pDCs before, from third week of BCG instillations mDCs were detected (Rossi et al., 2013). DC cells previously co-cultured with the pumc-91 BlCa cell line resulted in an impaired induction of T cell proliferation. Additionally, a decrease in the levels of T cell-derived cytokines (IL-2, IL-4, IL-6, IL-10, TNF-α, IFN-γ and IL-17A) was observed, compared to control DCs (Xiu et al., 2016), indicating that BlCa cells might induce DC dysfunction, failing to induce T cell responses (Xiu et al., 2016). In patient tissues, high-grade NMIBC and MIBC patients showed similar mature DCs (CD83⁺) levels in bladder peritumoral area and absent expression in intratumoral area (Viveiros et al., 2022).

B cells are important molecules in the adaptive immune response capable of produce both pro- and anti-inflammatory cytokines (Magatti et al., 2020). In silico analysis demonstrated that naive B cells were significantly lower in BlCa tumors than in control samples (Zhang et al., 2020). However, Ou Z et al. demonstrated that BlCa tissues had more B cells (CD20⁺), than the adjacent normal tissue samples (Ou et al. 2015). Considering high-grade NMIBC and MIBC patients, B cells were only present in bladder peritumoral areas (Viveiros et al., 2022). B cells were significanlty increased in MIBCs, and higher B cell levels were statistically associated with poor DSS (Viveiros et al., 2022). Moreover, Ou Z et al. showed that BlCa cell lines’ migration and invasion significantly increase after co-culture with B cells and in vivo, tumor infiltrating B cells could promote BlCa metastasis Ou et al. (2015).

Immune cells are major cytokines/chemokine producers, playing a role in initiating and triggering immune responses and recruitment of other cell populations to the tumor site. Thus, dysregulations in immune populations in the tumor, can then reflect in the cytokine production in the TME. Those alterations will not only impact in the recruitment and shaping of other immune cells, but also in shaping tumor cells. The impact of TME on driving tumor cell mechanisms that lead to evasion will define tumor development.

IL-8, also known as CXCL8, is an angiogenic factor associated with inflammation and tumorigenesis and it is considered a pro-inflammatory cytokine (Urquidi et al., 2012; Yao et al., 2020). This chemokine has a powerful leukocyte chemoattraction (Koçak et al., 2004; Jovanović et al., 2010), specially neutrophils attraction (Jovanović et al., 2010). Indeed, in inflammatory regions, IL-8 is responsible to attract and activate neutrophils (Bickel, 1993). Additionally, IL-8 promotes the adhesion of monocytes and neutrophils to endothelial cells, facilitating translocation to inflamed tissues (Gonzalez-Aparicio and Alfaro, 2018). IL-8 can be secreted by lymphocytes, neutrophils, macrophages and by several types of tumor cells (Ou et al., 2015). Furthermore, IL-8 plays an important role in promoting angiogenesis, since contributes to the growth and survival of endothelial cells (Tseng-Rogenski and Liebert, 2009). CXC chemokine receptor 1 (CXCR1) and CXC chemokine receptor 2 (CXCR2), also known as interleukin-8 receptor type beta (IL8RB), are IL-8 receptors, usually expressed in neutrophils and granulocytic myeloid-derived suppressor cells (GR-MDSC) (Miyake et al., 2019; Teijeira et al., 2020). When IL-8 binds to CXCR1 and CXCR2 activates serine/threonine kinases, protein tyrosines and Rho-GTPases, stimulating the expression of proteins related with cell proliferation, survival and cell invasion (Escudero-Lourdes et al., 2012).

In silico GSE32894 database, lower IL8 levels were associated with improved DSS (Chen et al., 2022). However, in The Cancer Genome Atlas (TCGA) database, it was demonstrated that higher IL8 levels were significantly associated with basal subtype (usually associated with advanced stage tumors and metastatic disease), comparing with luminal subtype (predominantly associated with papillary histopathological features) (McConkey and Choi, 2018; Chen et al., 2022) (Table 1).

IL-8 urinary protein concentration was found to be significantly higher in bladder tumor patients, comparing with healthy controls (Urquidi et al., 2012; Al-biaty, 2015; Kumari et al., 2017). Furthermore, a significant IL-8 increase was assessed in higher grade and in MIBC tumors, where recurrent disease showed higher IL-8 protein levels, compared with healthy control or newly diagnosed patients (Al-biaty, 2015; Kumari et al., 2017) (Table 1).

Reis ST et al. demonstrated that the majority of bladder tumors tissues underexpressed IL-8, comparing with controls (Reis et al., 2012). However, a significant association was established between high-grade tumors and higher IL8 levels (Reis et al., 2012). Moreover, pT1 and pT2 showed higher IL8 levels expression than pTa tumors, and recurrent disease patients demonstrated significant higher IL8 levels, compared to patients that not recurred (Reis et al., 2012) (Table 1).

It was also demonstrated in vitro that IL-8 is actually expressed by normal urothelial cells and promotes not only cellular growth, through AKT pathway, but also cellular survival in normal urothelial cells (Tseng-Rogenski and Liebert, 2009). Additionally, IL8/IL-8 levels were significantly higher in BlCa cell lines (J82 and TCCSUP) after co-culture with macrophages (Huang et al., 2020). Furthermore, studies in vitro suggest a relationship between IL-8 and BCG treatment, since this treatment promotes Ca²⁺ signaling stimulation and NF-kB activation, being responsible for an increase of IL-8 secretion (Ibarra et al., 2019) (Table 1).

According to the literature, in serum samples, IL-8 expression was significantly associated with poor CSS and shorter OS (Morizawa et al., 2018) (Table 1).

In vivo studies demonstrated that IL-8 is able to regulate BlCa tumorigenicity and metastasis formation, and higher IL-8 expression was correlated with higher tumor-induced neovascularization (Inoue et al., 2000). Furthermore, when nude mice implanted with 253J B-V and UMUC3 cell lines in the bladder cell wall were treated with ABX-IL8, an inhibitor of IL-8, it was observed a significant suppression in tumor growth (Mian et al., 2003) (Table 1).

Since IL-8 is upregulated in MIBC tumors (Al-biaty, 2015), and seems to promote tumor growth (Mian et al., 2003) and metastasis formation (Inoue et al., 2000), it suggests that it might play a crucial role in driving EMT. Until now, there are some studies focusing on how deregulation of IL-8 in BlCa might promote alterations in EMT-related molecules and which signaling pathways might be involved in BlCa. It is established that arsenic (As) exposure is a risk factor of BlCa (Escudero-Lourdes et al., 2012). UROtsa, an urothelial cell line, exposed to the arsenic metabolite monomethylarsonous [MMA (III)] undergo malignant transformation. MMA (III) exposure induced IL8/IL-8 overexpression, followed by an increase of CCND1, BCL2 and MMP9 (Escudero-Lourdes et al., 2012). In vivo, IL8 silencing induced a significant decrease of cell proliferation and of tumor formation, while, in vitro, was observed a downregulation of CCND1, BCL2 and MMP9 (Escudero-Lourdes et al., 2012). Furthermore, SVHUC1, a non-malignant BlCa cell line, demonstrated HER2 overexpression and an IL8/IL-8 activation upon exposure to As (Zhou et al., 2021). Consequently, IL-8 promoted extracellular signal-regulated kinase (ERK), AKT, and signal transducer and activator of transcription (STAT) 3 signaling activation, resulting in an evident influence in EMT, since the E-cadherin decreased, while Vimentin, Snail, Slug and Twist increased (Zhou et al., 2021). It was shown that a tight junction protein family member, occludin, regulated angiogenesis by controlling IL-8/STAT3 signaling pathway by STAT4 activation (Yang et al., 2022). Retz MM et al. showed that co-culture of B cells with the BlCa cell lines, TCCSUP, T24 and J82, increased bladder cell invasion and migration (Ou et al., 2015). The authors suggested that infiltrating B cells can promote IL-8 increase and, consequently, an increase of androgen receptor (AR), leading to MMP-1 and MMP-13 increase (Ou et al., 2015). Corroborating these findings, in vivo experiments showed that infiltrating B cells could increase BlCa cell invasion via increasing AR signal (Ou et al., 2015). Furthermore, it was demonstrated that IL-8 regulates MMP9 expression in 253J-P and 253J-BV cells lines (Inoue et al., 2000). Indeed, Mian BM el al. showed, in vitro, that IL-8 neutralization resulted in a decrease of MMP-2 and MMP-9 expression, in part, through NF-kB, and, consequently, promoted cell invasion decrease (Mian et al., 2003) (Table 1).

Monocyte chemoattractant protein -1/chemokine (C-C motif) ligand 2 (MCP-1/CCL2) plays a crucial role in immune responses, regulating infiltration and migration of several immune cells (Xu et al., 2021). CCL2 is a potent chemoattractant for monocytes/macrophages (Li and Tai, 2013) and can activate dendritic cells, memory T cells and basophils (Chiu et al., 2012; Xu et al., 2021). CCL2 is secreted by activated macrophages, fibroblasts, vascular smooth muscle, lymphocytes, and tumor cells (Amann et al., 1998). Usually binds to C-C chemokine receptor type 2 (CCR2), but it also binds to CCR4 (Zhang et al., 2010; Gao et al., 2019). CCL2 expression can be activated by several growth factors and cytokines, such as platelet-derived growth factor (PDGF), TNF-α, IL-1β and IFN-γ (Li and Tai, 2013). Overall, according to the literature, CCL2 in the TME seems to mainly contributes for tumor progression and metastasis formation (Jin et al., 2021).

In silico data analysis showed that CCL2 expression was significantly lower in BlCa patients than the controls (Li et al., 2021). Additionally, higher CCL2 levels were associated with better DFS (Li et al., 2021). In patient tissues, CCL2/CCL2 was described to be significantly higher in tumors, compared with normal and adjacent tissues (Wang et al., 2017). Considering NMIBC and MIBC patients, higher CCL2 levels significantly correlated with higher grade, stage and lymph node metastasis (Gao et al., 2019). Particularly, considering only MIBC patients, a positive CCL2 expression in tumor cells was associated with poor mean OS, DSS and recurrence-free survival (RFS), while expression of CCL2 in immune cells, was associated with longer OS, DSS, and RFS (Eckstein et al., 2020). The role of CCL2 in immune cells is dependent on the lymph node patient’s status, as CCL2 in N0 was linked to a good prognosis while N1+N2 was associated with poor prognosis (Eckstein et al., 2020) (Table 1).

In urine samples from BlCa patients, advanced stages (pT2-pT4) presented three to fourfold higher mean concentration, comparing with pT1 stage tumors (Amann et al., 1998) (Table 1).

In vitro, it was demonstrated that higher CCL2 levels were associated with high-grade BlCa cell lines (T24 and J82), while low-grade BlCa cell lines (SVHUC1, RT4 and TSGH8301), showed lower CCL2 levels (Chiu et al., 2012). In addition, higher CCL2 levels were produced in MB49 and MBT-2 cisplatin-resistant cells lines, comparing with parental BlCa cell lines (Takeyama et al., 2020). So far, there is a lack of information about CCL2 expression in plasma, in in vivo and in serum of BlCa patients (Table 1).

Besides, in BlCa, the knowledge about the impact of CCL2 in EMT induction and the signaling pathways activated by CCL2 promoting EMT, is still poor, although some studies have been arising. Co-culture of mast cells (HMC-1) with the BlCa cell lines, T24 and 647V, resulted in an increase of the estrogen receptor beta (ERβ) levels and of CCL2 levels in both cell types (Rao et al., 2016). After co-culture, higher CCL2 levels promoted EMT, driving stimulation of MMP-9 expression and enhanced N-cadherin, Twist, Snail and Vimentin expression levels, resulting in higher BlCa cell lines invasion abilities (Rao et al., 2016) (Table 1). Long noncoding RNA Lymph Node Metastasis Associated Transcript 1 (LNMAT1), overexpressed in BlCa tissues comparing with normal adjacent tissues, can directly interact with heterogeneous nuclear ribonucleoprotein L (hnRNPL), resulting in an increase of the H3 lysine four trimethylation (H3K4me3) of the CCL2 promoter (Chen et al., 2018). CCL2 overexpression resulted in increased TAM recruitment. Macrophage activation resulted in secretion of lymphangiogenic growth factor (VEGF-C) to the bladder TME, promoting lymphangiogenic and lymphatic metastasis (Chen et al., 2018). In mouse BlCa cell line MBT2, CCL2-CCR2 interaction may facilitate migration by phosphorylating paxillin y118 through a protein kinase C (PKC)-dependent mechanism (Chiu et al., 2012).

CXCL1, also known as MGSA, is a powerful neutrophil chemoattractant chemokine (De Filippo et al., 2013; Boro and Balaji, 2017), interacting with the CXCR2 receptor (Kawanishi et al., 2008). CXCL1 plays a double role in immune responses, since it can recruit and activate neutrophils to the infection area, but can also activate the release of several proteases and reactive oxygen species (ROS) that will result in cell death (Sawant et al., 2016). This chemokine plays important roles in several tumor models, promoting cell migration and invasion (Cheng et al., 2011; Wang et al., 2018). Mast cells, alongside with macrophages are able to produce CXCL1 (De Filippo et al., 2013).

In silico, UALCAN analysis showed higher CXCL1 transcript levels in BlCa samples compared with normal bladder mucosa tissues, and, according to GEPIA and GEO database analysis, higher CXCL1 was significantly associated with shorter OS (Sun et al., 2021b) (Table 1).

While benign or normal bladder tissues showed absent CXCL1 levels, higher CXCL1 levels were significantly associated with more undifferentiated tumors and MIBC (Kawanishi et al., 2008; Miyake et al., 2013). Consequently, high amounts of CXCL1 contributed to poor DSS and poor OS (Miyake et al., 2013). Additionally, increased CXCL1 levels in the tumors promoted the recruitment of CAFs and were associated with higher number of TAMs (Miyake et al., 2016) (Table 1).

In in vitro studies, higher CXCL1 expression was observed in the most aggressive BlCa cell lines (UMUC3, 5637 and T24) (Kawanishi et al., 2008). Moreover, CXCL1 could enhance the invasive ability of BlCa cell lines (Kawanishi et al., 2008; Miyake et al., 2019). Additionally, CXCL1 influenced the angiogenesis process and tumor vasculature, since tube structures were significantly lower after treatment with conditioned media from CXCL1-knockdown T24 cells (Miyake et al., 2019). Furthermore, higher CXCL1 amounts were obtained with MB49, MBT-2 and T24 cisplatin-resistant cells lines, in comparison with parental BlCa cell lines (Takeyama et al., 2020) (Table 1).

In vivo, it was shown that CXCL1 secreted by TAMs and CAFs enhanced bladder tumor cell attachment to the bladder wall, consequently inducing tumor growth (Miyake et al., 2016). Moreover, by using T24 cell xenografts treated with HL2401, a CXCL1 inhibitor, it was observed a significant increase in the apoptotic index, but a significant decrease in microvessel density and a reduction in proliferation (Miyake et al., 2019).

In liquid biopsies, CXCL1 urinary protein concentrations were significantly higher in BlCa patients comparing with patients without BlCa (Kawanishi et al., 2008; Burnier et al., 2015). Importantly, a significant increase was obtained in stages pT1-pT4, comparing with pTa (Kawanishi et al., 2008) (Table 1).

Information regarding CXCL1 expression in serum and in plasma of BlCa patients is still lacking (Table 1). Also, the role that CXCL1 might have in driving EMT is little explored, as well as the signaling pathways activated by CXCL1 to induce EMT in BlCa. However, it is known, that in vivo, overexpression of CXCL1 by TAMs and CAFs, promoted alterations in BLCa EMT, decreasing E-cadherin membrane expression, while increasing MMP-2 expression (Miyake et al., 2016) (Table 1). Furthermore, in tissues, a significant correlation was established between CXCL1 and MMP-13 (Kawanishi et al., 2008) (Table 1). In silico analysis, using LinkedOmics database, also showed that microRNA (miR)-200a, an important hallmark in EMT (Adam et al., 2009), interacts with CXCL1 (Sun et al., 2021b) (Table 1).

CXCL12, also known as stromal cell-derived factor 1 (SDF-1), or pre-B cell stimulating factor (PBSF) (Yang et al., 2015), interacts with CXCR4 and CXCR7 receptors (Shen et al., 2013; Zhang et al., 2018). CAFs are able to secrete CXCL12, being essential for CD8⁺ T cells recruitment (Du et al., 2021c). This chemokine participates in the homeostatic regulation of leukocyte trafficking and tissue regeneration (Barinov et al., 2017). CXCL12 is also described to be involved in tumor growth, angiogenesis and tumor cell intravasation (Chang et al., 2020).

in silico analyses (GEO, TCGA, ONCOMINE and UALCAN) showed that CXCL12 was significantly decreased in BlCa samples, comparing with the controls (Sun et al., 2021b; Du et al., 2021c). On the other hand, higher CXCL12 expression was significantly associated with more advanced stages, worse prognosis, and more lymph node metastasis (N2 showed higher CXCL12 than N0) (Sun et al., 2021b; Liu et al., 2021).

In accordance with in silico data, Du Y et al. showed a CXCL12 reduction in BlCa patient tissues comparing with the normal tissues Du et al. (2021c), while Yang DL et al. showed a significantly higher expression of CXCR4/CXCL12 in BlCa tissues and no expression in normal tissues Yang et al. (2015). It was demonstrated that CXCL12 positively associated with tumor grade and stage in BlCa patient tissues, being CXCL12 expression more intense in recurrent patients (Batsi et al., 2014). Moreover, Yang DL et al. showed that CXCR4/CXCL12 levels strongly associated with tumor progression and invasion, and CXCL12 transcript levels in tumor tissues increased with tumor aggressiveness.

There are several CXCL12 mRNA variants depending on alternative splicing (Gosalbez et al., 2014; Chang et al., 2020). CXCL12-α, CXCL12-β and CXCL12-γ are some of the variants, presenting the same first three exons (Chang et al., 2020). According to the literature, CXCL12-α has the strongest affinity to CXCR4, followed by CXCL12-β and CXCL12-γ (Chang et al., 2020). By qPCR, it was demonstrated that CXCL12-α and CXCL12-β levels were higher in metastatic patient tissues compared to non-metastatic patient tissues (Gosalbez et al., 2014). Moreover, only CXCL12-β was significantly higher in tumor patients than normal samples (Gosalbez et al., 2014). In urine, CXCL12-γ was not detected, but CXCL12-α levels were significantly lower in patients with low-grade compared to controls, while CXCL12-β levels were significantly higher in high-grade than the controls (Gosalbez et al., 2014).

There is no information regarding CXCL12 expression in plasma and in serum, similarly to CCL2 and CXCL1 (Table 1). Up till now, CXCL12 has been described to have an important role in regulating some EMT-related molecules in BlCa. Additionally, studies on the signaling pathways that might be activated by this chemokine started to arise. In vitro, it was shown that CXCL12 was involved in cell invasion and migration (Retz et al., 2005; Shen et al., 2013). CXCR4 and CXCL12 binding drives the induction of STAT3 phosphorylation (Shen et al., 2013), an important molecule in promoting BlCa growth and survival, and able to work as a transcription factor regulating EMT (Chen et al., 2008; Jin, 2020) (Table 1). This alteration in migration might occur due to an association of CXCR4/CXCL12 with cytoskeletal reorganization, specifically, with a redistribution of F-actin stress fibers (Retz et al., 2005). A study from Zhang T et al. reinforced these findings, since SW780 treated with AMD34635, a CXCR4 inhibitor, exhibited growth and colony formation supression, as well as, inhibiton on migration and invasion (Zhang et al., 2018). In addition, in vivo, it was demonstrated that tumors with AMD3465-treatment showed slower growth and lower weight than tumors treated with the vehicle (Zhang et al., 2018). Additionally, in vitro, it was also demonstrated that molecular alterations occurred, with a decrease of β-catenin, MMP-2 and c-Myc expression and with an increase in E-cadherin levels (Zhang et al., 2018) (Table 1). However, the effect of AMD3465 was reversed when CXCL12 was added, inducing E-cadherin downregulation and c-Myc upregulation (Zhang et al., 2018) (Table 1). Moreover, SW780 cells treated with FH535, a β-catenin antagonist, also decrease cell proliferation, colony formation, migration and invasion, being these effects once again reverse by CXCL12 treatment. Thus, suggesting that CXCR4/CXCL12 play an important role in regulated β-catenin expression in BlCa progression (Zhang et al., 2018) (Table 1).

IL-6 is a pro-inflammatory interleukin (Chen et al., 2013; Morizawa et al., 2018) known to play a major role in inflammatory responses (Chen et al., 2013; Yao et al., 2020), as well as in the maturation of B cells (Andrews et al., 2002; Miyake et al., 2019). IL-6 binds to the receptor IL6-R, present in the extracellular membrane, or secreted in a soluble form (IL-6sR) (Andrews et al., 2002). IL-6 is mainly produced by tumor-infiltrating immune cells, such as T cells and macrophages, by tumor cells, by healthy endothelial tissues, by epithelial cells and by muscle cells (Andrews et al., 2002; Rossi et al., 2015; Schuettfort et al., 2022).

In tissues, Chen MF et al. showed that IL-6/IL6 expression was higher in BlCa tissues, comparing with non-malignant tissues (Chen et al., 2013). The authors demonstrated that non-malignant tissues exhibited IL-6 expression, but in lower levels, compared to early stages, while IL-6 higher levels were mostly associated with MIBC tissues (Chen et al., 2013) (Table 1).

In silico analysis, revealed that IL6 transcript levels were significantly increased in higher stages (stages III and IV), comparing with lower stages (stages I and II) (Goulet et al., 2019). Moreover, IL6 was significantly enhanced in high-grade patients, comparing with low-grade patients (Goulet et al., 2019) (Table 1).

In urine samples, IL-6 levels were significantly higher in advanced stage patients (pT3-pT4), comparing with patients with early stage tumors or non-malignant samples (Chen et al., 2013). Kumari N et al. showed that higher IL-6 concentration was significantly associated with lower disease grade Kumari et al. (2017). Furthermore, it was demonstrated that IL-6 levels in urine were associated with shorter OS (Morizawa et al., 2018) (Table 1).

Using preoperative plasma samples, Schuettfort VM et al. and Andrews B et al. demonstrated that IL-6 and IL-6sR were significantly higher in patients with advanced stages, lymph vascular invasion and lymph node metastasis Andrews et al. (2002), Schuettfort et al. (2022). Dmytryk V et al. also observed significantly higher IL-6 leveles in pT3-pT4 samples, comparing with control samples Dmytryk et al. (2020). Moreover, patients with recurrent disease or patients who deceased due to BlCa disease presented higher IL-6 and IL-6sR levels (Schuettfort et al., 2022). Higher IL-6 and IL-6sR levels were associated with poor RFS, CSS and OS (Schuettfort et al., 2022). Andrews B et al. showed that plasma IL-6 levels were significantly higher in BlCa than in healthy patients, however IL-6sR levels did not present statitiscal differences bteween the two groups (Andrews et al., 2002) (Table 1).

In serum BlCa samples, collected prior to surgery, IL-6 levels were significantly higher in recurrent patients, comparing with non-recurrent patients and were significantly associated with poor RFS (Kumari et al., 2017). Similar to IL-8, IL-6 expression was significantly associated with shorter CSS (Morizawa et al., 2018). However, Yang G et al. described a descrease of IL-6 levels in T2-T4 patient samples, comparing with Ta-T1 samples and healthly controls (Yang et al., 2017) (Table 1).

Regarding the literature, BlCa cell lines produced high IL-6 levels, while normal cell lines expressed only low IL-6 levels (Okamoto et al., 1997). Upon IL-6 treatment, BlCa cell lines (253J, RT4 and T24) presented enhanced cellular growth, comparing with normal cell lines (Okamoto et al., 1997). Moreover, the cell growth was significantly inhibited upon anti-IL-6 neutralizing antibody treatment, suggesting that IL-6 provides autocrine growth advantages to the BlCa cell lines (Okamoto et al., 1997). Additionally, Yeh CR et al. suggested that, in vitro, ERα overexpression in fibroblasts may increase BlCa cell invasion through IL-6 expression in BlCa cells (Yeh et al., 2015). Miyake M et al. demonstrated, in vivo and in vitro, that CXCL1 had an important impact in BlCa tumor growth, since promoted IL-6 induction and repressed tissue inhibitor of metalloproteinase 4 (TIMP4) inhibition Miyake et al. (2019). Chen MF et al. showed that IL6 silencing contributed to a decrease in tumor invasion and tumor growth/proliferation, both in vivo and in vitro (HT1197 and HT1376 cell lines) Chen et al. (2013).

Overall, IL-6 has been described to be upregulated in advanced BlCa patients (Chen et al., 2013; Goulet et al., 2019) and in lymph node metastasis (Andrews et al., 2002; Schuettfort et al., 2022). Thus, the association between IL-6 and EMT induction starts to be studied in BlCa, along with which signaling pathways can be activated by IL-6. Indeed, IL6 overexpression in HT1376 cells promoted a decrease in N-cadherin and Vimentin levels, while the IL6 knockdown in T24 cells led to a decrease in E-cadherin, but an increase in N-cadherin and Vimentin levels (Tsui et al., 2013) (Table 1). However, it was demonstrated that IL6 silencing was able to increase E-cadherin levels, but decreased MMP-9 levels and attenuated angiogenesis, since it led to a decrease of CD31 and vascular endothelial growth factor (VEGF) levels (Chen et al., 2013) (Table 1). EMT-player alterations, induced by IL-6, might be regulated by STAT3 signaling pathway activation (Chen et al., 2013) (Table 1). In patient tissues, it was demonstrated a significant positive correlation between p-STAT3 Y705 and IL-6, and a significant negative correlation between p-STAT3 Y705 and E-cadherin, suggesting that E-cadherin expression might be inhibited by IL6-STAT3 signaling pathway (Chen et al., 2020). In vitro, it was demonstrated that IL-6-induced STAT3 is able to target TWIST promoter, modulating EMT and BlCa cell invasion (Yao et al., 2020).

TGF-β1 is the most well studied isoform and its receptors are membrane serine-threonine kinase receptors I and II (TGF-βRI and TGF-βRII) (Kim et al., 2001). This cytokine has been described as playing a dual role in tumorigenesis, displaying a tumor suppressor role in normal cells or in early tumor stages, inducing cell cycle arrest and apoptosis, while in late stages can promote cell motility and invasion (Eder et al., 1997; Jakowlew, 2006; Lebrun, 2012; Stojnev et al., 2019). Overall, TGF-β1 is mainly released by regulatory T cells (Efiloğlu et al., 2020) and CAFs (Ao et al., 2007; Yu et al., 2014; Yeh et al., 2015), M2 macrophages (Horibe et al., 2021) and MDSC (Groth et al., 2019). TGF-β1 can activate both SMAD-dependent or SMAD-independent signaling (Hata and Chen, 2016). TGFRβII point mutations have been reported, not only in the BlCa cell line T24, but also in BlCa patients, being associated with higher pathologic T category and tumor grade (Bian et al., 2013).

In silico analysis, it was demonstrated that TGFB1 is upregulated in MIBC compared to NMIBC and patients with higher TGFB1 expression presented higher risk of death, lower DFS and lower OS (Zou et al., 2019) (Table 1).

In BlCa patient samples, TGF-β1 is expressed in normal urothelium, although at lower levels (Yang et al., 2018; Zou et al., 2019). Within tumors, higher TGF-β1 levels were significantly associated with higher tumor stage and grade and correlated with cancer-specific death (Kim et al., 2001; Yang et al., 2018; Stojnev et al., 2019; Zou et al., 2019). On the other hand, although Miyamoto H et al. also found that TGFB1 transcript levels were higher in tumor tissues, than in normal samples, TGFB1 transcript levels were significantly associated with low-grade and stage Miyamoto et al. (1995) (Table 1).

In BlCa patient serum samples, Efiloğlu Ö et al. described that higher TGF-β1 was associated with a low risk of tumor progression (Efiloğlu et al., 2020). Indeed, Eder IE et al., using serum samples, mentioned that TGF-β1 levels were significantly lower in T4 tumors than superficial and invasive (T2-T3) tumors Eder et al. (1997). However, Eder IE et al. demonstrated that superficial tumors (Ta-T1) had significantly TGF-β1 higher levels, than normal samples (Eder et al., 1997). Another study from Eder IE et al. mentioned that serum TGF-β1 were elevated in the most aggressive BlCa cases compared to controls, and in the most undifferentiated tumors, than with lower grade tumors (Eder et al., 1996) (Table 1).

Also in preoperative plasma, TGF-β1 levels were significantly higher in MIBC patients with regional and distant lymph node, comparing with non-metastatic MIBC and controls (Shariat et al., 2001). An increase of TGF-β1 was found in MIBC, comparing with less aggressive tumors, with patients with higher TGF-β1 demonstrating increased risk of disease recurrence and mortality (Shariat et al., 2001). On the other hand, no significant differences were found between controls and patients with early stages (Shariat et al., 2001) (Table 1).

In urine samples, it was observed a significantly higher number of BlCa samples expressing TGF-β1 comparing with chronic cystitis disease cases or the control group (Helmy et al., 2007) (Table 1).

In vivo, it was observed an increase of, not only in tumor size, but also in tumor weight (Zou et al., 2019) when the 5637 cell line overexpressing TGF-β1 was transplanted into mice, compared with the parental cell line (Zou et al., 2019) (Table 1).

As mentioned above, TGF-β1 is an important inducer and regulator of EMT (Stojnev et al., 2019). EMT-related molecules regulated by TGF-β1 and the signaling pathways activated by this cytokine have been well described in several models, including in BlCa. Both in vitro and in vivo, an increase of TGF-β1 reflected in an upregulation of EMT-related molecule levels, such as Slug, Vimentin, Snail, MMP-2, MMP-9 and E-cadherin (Zou et al., 2019). Additionally, TGF-β1 has been associated with proliferation, colony formation, migration and invasion in BlCa cell lines (Bian et al., 2013; Zhang et al., 2016; Zou et al., 2019). HTB9 and T24 cell lines treated with TGF-β1 resulted in E-cadherin/CDH1 decrease, and a N-cadherin/CDH2 and Vimentin/VIM increase (Chen et al., 2014). Upon TGF-β1 treatment, it was shown miR-200b downregulation and MMP-16 upregulation, due to miR-200b targeting of MMP-16 (Chen et al., 2014). TGF-β1 treatment of T24 and BIU87 BlCa cell lines resulted in increased fascin1 levels, an important molecule in tumor migration and invasion (Zhang et al., 2016). Finally, AY-27, a rat cell line, treated with TGF-β1 resulted in alterations in morphology, with the increase of spindle shaped cells, while the polygonal shaped cells decreased, as well as cell-to-cell contact (Koo et al., 2010). In Smad-dependent signaling, it occurs recruitment and phosphorylation of SMAD2 and SMAD3 (Heldin et al., 2012; Gonzalez and Medici, 2014; Papageorgis, 2015; Gupta et al., 2016). Then, SMAD4 is recruited, forming a trimeric complex capable to be translocated to the nucleus (Bian et al., 2013; Gonzalez and Medici, 2014; Gupta et al., 2016). In BlCa samples, Smad2 and Smad4 expression were associated with low-grade and superficial tumors, and better overall survival of the patients (Stojnev et al., 2019). However, it was observed an increase of p-SMAD2 in invasive bladder tumors (Gupta et al., 2016). Knockdown of PPM1A, an antagonist of TGF-β signaling by dephosphorylating TGF-β-activated Smad2/3, resulted in an increase in p-Smad2/3 levels upon TGF-β1 treatment, in 5637 and T24 cell lines (Geng et al., 2014).