Evidence has revealed that miR-26a is critically involved in osteosarcoma progression via regulating several downstream targets (Song et al., 2014; Liu et al., 2018). Downregulation of miR-26a was observed and associated with poor prognosis in osteosarcoma patients (Song et al., 2014). For example, miR-26a blocked the migration and invasion of osteosarcoma cells via directly inhibiting HMGA1 (Liu et al., 2018). Similarly, miR-26a retarded the migratory and invasive capacity of osteosarcoma cells via repressing EZH2 expression (Song et al., 2014). Tan et al. reported that miR-26a attenuated cell proliferation via inhibiting IGF-1 expression in osteosarcoma cells (Tan et al., 2015). Li et al. found that miR-26a could reverse doxorubicin resistance via inhibiting MCL1 in osteosarcoma cells (Li and Ma, 2021). Surprisingly, one study reported that miR-26a might be an oncogene in osteosarcoma. Qu et al. found that miR-26a enhanced cell growth and tumor metastasis via regulating the Wnt/β-catenin pathway by inhibiting GSK-3β in osteosarcoma (Qu et al., 2016). Another study showed that miR-26a repressed stem cell-like properties via inhibition of Jagged-1 in osteosarcoma (Lu et al., 2017). Notably, decreased expression of miR-26a was linked to lung metastasis and poor survival in patients with osteosarcoma (Lu et al., 2017). Moreover, lower expression of miR-26a existed in osteosarcoma CSCs, and lentivirus-mediated upregulation of miR-26a reduced the expression of stem cell biomarkers, including SOX2, CD133, OCT3/4, Nanog, and nucleostemin in osteosarcoma cells (Lu et al., 2017). ZOS and 143B cells formed smaller and fewer sarcosphere and had a reduction of the ALDH activity after infection with lentiviruses carrying miR-26a. Moreover, miR-26a suppressed the expression of Jagged-1, and led to inhibition of tumor cell growth in vitro and in vivo (Lu et al., 2017).

Zou et al. revealed that miR-34a expression was lower in osteosarcoma stem-like cells, and overexpression of miR-34a reduced the expression of the stem cell markers and retarded the osteosphere formation (Zou et al., 2017). Zhang et al. discovered that miR-34a worked as a suppressor in regulation of osteosarcoma dedifferentiation into CSCs via inhibition of Sox2 (Zhang et al., 2018). Liang et al. reported that miR-34a was increased after DNMT1 downregulation, leading to suppression of stemness markers expression, including CD133, CD44, Oct4, Sox2, Bmi1 and ABCG2 in osteosarcoma stem-like cells (Liang et al., 2019b). Consistently, overexpression of DNMT1 reduced the expression of miR-34a and promoted the expression of stemness markers in osteosarcoma stem-like cells (Liang et al., 2019b). Moreover, Liang et al. found that isovitexin, a natural flavonoid, reduced the expression of CD133, CD44, ALDH1 and ABCG2 at mRNA levels in osteosarcoma sphere cells, leading to suppression of tumor growth and induction of apoptosis. Mechanistic study showed that isovitexin reduced DNMT1 expression and activity, upregulated miR-34a and attenuated the expression of Bcl-2 in osteosarcoma sphere cells (Liang et al., 2019a).

Evidence demonstrated that miR-143 is linked to the survival of OS cells with ALDH1+CD133+ and participated in drug resistance (Zhou et al., 2015). Loss of miR-143 expression was associated with poor survival of OS patients. Overexpression of miR-143 overcame drug resistance via inhibition of ATG2B, LC3-1 and Bcl-2 in U2OS- and SaOS-2-resistant cells (Zhou et al., 2015). In addition, miR-143-3p is involved in osteosarcoma development and progression. MiR-143-3p was identified as a potential marker for diagnosis and prognosis in osteosarcoma patients, because low expression of miR-143-3p was correlated with tumor size, stage and metastasis (Yang et al., 2020). Sun et al. showed that miR-143-3p repressed cell proliferation and invasion via suppression of FOSL2 in osteosarcoma (Sun et al., 2018). Hou et al. observed that miR-143-3p reduced cell growth, migratory and invasive capacity via attenuation of MAPK7 expression in osteosarcoma (Hou et al., 2019). Han et al. uncovered that ectopic expression of miR-143-3p blocked stemness features in osteosarcoma cells, including CD44, Oct4, Nanog and Notch1 (Han et al., 2020). Moreover, miR-143-3p inhibited KIAA1429 expression via binding with its 3′-UTR in U2OS and 143B cells (Han et al., 2020). Furthermore, miR-143-3p suppressed proliferation and invasiveness in a KIAA1429-dependent manner in osteosarcoma cells (Han et al., 2020).

Wei et al. reported that miR-1247 repressed cell viability and blocked tumor metastasis via inhibiting NRP1 expression and mediating Wnt/β-catenin pathway in OS (Wei et al., 2019). Evidence showed that miR-1247 was downregulated in OS cells with CD117+Stro-1+ (Zhao et al., 2015). Moreover, miR-1247 bound to MAP3K9 and inhibited its expression in OS cells. MAP3K9 facilitated proliferation of OS cells and stem cell sphere formation in CD117+Stro-1+ cells (Zhao et al., 2015). Restoration of miR-1247 reduced the clonogenic growth and suppressed tumor spheres in OS cells (Zhao et al., 2015). This study implied that miR-1247 could be involved in regulation of the self-renewal of OS CSCs.

One investigation revealed the association between miR-133a expression and osteosarcoma-initiating cells (Fujiwara et al., 2014). This study found that 20 miRNAs were upregulated in CD133 (high) OS cells, including miR-133a (Fujiwara et al., 2014). Moreover, miR-133a promoted cell invasion in CD133 (high) OS cells. Moreover, OS patients with poor prognosis have a high expression of miR-133a (Fujiwara et al., 2014). Chemotherapeutic treatment increased the expression of miR-133a in OS cells. Furthermore, miR-133a exerted its functions in part via inhibition of SGMS2, UBA2, SNX30 and ANXA2 in OS cells (Fujiwara et al., 2014). Therefore, miR-133a could be involved in development and metastasis of OS CSCs.

miR-382 has been reported to regulate tumor growth and metastasis in osteosarcoma cells (Xu et al., 2014). Osteosarcoma patients with lower expression of miR-382 had a poor chemoresponse and poor survival (Xu et al., 2014). Ectopic expression of miR-382 reduced growth and chemoresistance of osteosarcoma cells via attenuating KLF12 and HIPK3 (Xu et al., 2014). miR-382-5p, a miRNA species of miR-382, was reported to govern hematopoietic stem cell differentiation via the inhibition of MXD1 (Zini et al., 2016). One study revealed that miR-382 was involved in regulation of CSC populations in colorectal cancer spheroid cells (Rengganaten et al., 2020). miR-382 reduced metastasis and relapse via suppression of YB-1 in osteosarcoma cells (Xu et al., 2015). The upregulation of miR-382 repressed EMT and lung metastasis as well as reduced the population of CSCs (CD133 high) in LM-5 and M132 osteosarcoma cells (Xu et al., 2015). In keeping with this result, knockdown of miR-382 induced EMT and metastasis and elevated the percentage of CSCs in SaOs-2 and HuO9 osteosarcoma cells (Xu et al., 2015). Consistently, the numbers of ALDH1-positive cells were changed after miR-382 modulation. Notably, miR-382 retarded the capacity of osteosarcoma cells to form osteospheres (Xu et al., 2015). The clinical data demonstrated that lower expression of miR-382 was existed in highly metastatic osteosarcoma cells and relapsed osteosarcoma specimens. Moreover, miR-382 expression level was linked to relapse and survival in patients with osteosarcoma. Furthermore, ectopic expression of miR-382 blocked CSC-mediated tumor formation in mice (Xu et al., 2015). Notably, miR-382 in combination with doxorubicin blocked disease relapse in osteosarcoma in nude mice. Mechanistically, miR-382 controlled EMT, stemness and tumor metastasis and relapse via inhibiting YB-1 (Xu et al., 2015).

Zhang et al. observed that miR-29b-1 decreased proliferation and migration of OS cells via blocking the expression of VEGF (Zhang et al., 2014). Zhu et al. found that miR-29b exerted antitumor activity in OS via modulation of CDK6 (Zhu et al., 2016). Xu and others reported that miR-29 family targeted COL3A1 and Mcl-1 and increased methotrexate sensitivity in OS cells (Xu et al., 2018). Moreover, miR-29b was reported to sensitize OS cells to doxorubicin via suppressing MMP-9 (Luo et al., 2019). Overexpression of miR-29b increased the radiosensitivity of OS cells via targeting PTEN/Akt/Sp1 pathway (Kim et al., 2020). One research dissected that miR-29b-1 repressed proliferation, self-renewal and overcame chemoresistance in 3AB-OS CSCs (Di Fiore et al., 2014). miR-29b expression was downregulated in 3AB-OS CSCs (Di Fiore et al., 2013), and overexpression of miR-29b-1 impaired proliferation, sarcosphere ability and colony formation ability (Di Fiore et al., 2014). Upregulation of miR-29b-1 sensitized chemotherapeutic drug efficacy in 3AB-OS cells. Moreover, miR-29b-1 reduced stemness properties via suppression of Oct3/4, Sox2 and Nanog in 3AB-OS CSCs (Di Fiore et al., 2014). Recently, soft substrate inhibited miR-29b expression and upregulated Spin one expression, leading to activation of PI3K/Akt and STAT3 pathways, which resulted in self-renewal, differentiation and drug resistance in OS cells (Li S. et al., 2020).

Emerging evidence has revealed that miR-335 overexpression retarded invasion and migration of osteosarcoma cells via repressing ROCK1 and SNIP1 expression (Wang et al., 2013; Xie et al., 2019). LncRNA TUG1 enhanced invasion and migration of OS cells via sponging miR-335-5p and upregulating ROCK1 (Wang et al., 2017b). LncRNA DANCR enhanced ROCK-1-induced proliferation and motility of OS cells via sponging miR-335-5p and miR-1972 (Wang et al., 2018). LncRNA LOC100129620 increased proliferation and migration via interacting with miR-335-3p and regulating CDK6 in OS cells (Chen et al., 2021). LncRNA CRNDE elevated OS progression by suppression of miR-335-3p (Yu et al., 2021). Upregulation of miR-335 induced apoptosis and attenuated cell viability via inhibition of survivin expression in OS cells (Liu et al., 2016). Clinically, the expression of miR-335 was lower in OS tissues compared with normal control tissues (Wang et al., 2013; Liu et al., 2016). Notably, lower expression of miR-335 was positively correlated with advanced clinical stage and distant metastasis (Wang et al., 2017a). Guo et al. reported that the downregulation of miR-335 was reported in osteosarcoma stem cells (Guo et al., 2017). Furthermore, miR-335 inhibited stem cell-like properties via suppression of POU5F1 in osteosarcoma (Guo et al., 2017). miR-335 upregulation inhibited the expression of CD117, Stro-1, and Sox2 in osteosarcoma cells. Inhibition of miR-335 enhanced stem cell-like properties and increased invasion of osteosarcoma cells. Moreover, miR-335 overexpression increased sensitivity of cisplatin in osteosarcoma cells (Guo et al., 2017).

Wang et al. reported that TGF-β-triggered EMT reduced the expression of miR-499a because Snail1 and Zeb1 bound with miR-499a promoter (Wang et al., 2019). Upregulation of miR-499a reduced TGF-β-mediated erlotinib resistance via inhibition of SHKBP1 in CD166 + OS CSCs (Di Fiore et al., 2016). The high ratio of the SHKBP1 and miR-499a were associated with EMT and erlotinib resistance in OS samples (Di Fiore et al., 2016). This study indicated that miR-499a might be involved in drug resistance in OS CSCs.

One research showed that the expression of let-7days miRNA was decreased in the 3AB-OS CSCs (Di Fiore et al., 2013). Upregulation of let-7d inhibited cell proliferation via suppressing the expression of CCND2 and E2F2 and upregulating p21 and p27 expression in 3AB-OS CSCs (Di Fiore et al., 2016). Moreover, overexpression of let-7d reduced sarcosphere capacity and attenuated the expression of several stem markers, including Sox2, Lin28B, Oct3/4, Nanog, and HMGA2, in 3AB-OS CSCs (Di Fiore et al., 2016). Furthermore, overexpression of let-7d reduced vimentin expression and N-cadherin expression, but increased E-cadherin expression, leading to mesenchymal to epithelial transition (Di Fiore et al., 2016). Interestingly, overexpression of let-7days elevated the expression of CXCR4, MMP-9 and VersicanV1, resulting in promotion of migration and invasion in 3AB-OS CSCs (Di Fiore et al., 2016). Moreover, upregulation of let-7d increased resistance to chemotherapy drugs, which was associated with downregulation of caspase-3 and upregulation of Bcl-2 expression in 3AB-OS CSCs (Di Fiore et al., 2016).

Recently, several studies identified that DANCR was increased in osteosarcoma tissues and tumor cell lines. High expression of DANCR was linked to tissue typing and TNM stage as well as metastasis in osteosarcoma patients (Jiang et al., 2017; Wang et al., 2018; Zhang W. et al., 2020). One study revealed that deficient of DANCR suppressed growth and autophagy, and triggered apoptosis via sponging miR-216a-5p and increasing the expression of SOX5 (Pan et al., 2020). Moreover, DANCR inhibited migration and invasion via targeting miR-149 and its downstream MSI2 in osteosarcoma (Zhang W. et al., 2020). In addition, DANCR acted as a ceRNA to sponge miR-335-5p and miR-1972, leading to inhibition of ROCK1 expression and depression of proliferation and motility of osteosarcoma cells (Wang et al., 2018). Jiang et al. reported that DANCR decoyed miR-33a-5p and upregulated AXL expression, contributing to tumor growth, migration, invasion and lung metastasis (Jiang et al., 2017). Mechanistically, DANCR stimulated tumor malignant phenotype via enhancement of CSCs features, which might be due to activation of PI3K/Akt signaling pathway in osteosarcoma (Jiang et al., 2017). Yuan et al. reported that DANCR promoted cell stemness property via derepressing CTNNB1 in hepatocellular carcinoma (HCC) cells (Yuan et al., 2016). DANCR expression was high in HCC cells with stem-like features (Yuan et al., 2016). DANCR depletion suppressed expression of several CSC markers, such as CD44, ABCG2, and ALDH1 in TNBC cells (Sha et al., 2017). In lung cancer cells, DANCR overexpression increased cell stemness via decoying miR-216a expression and subsequent activation of Wnt/β-catenin axis (Yu et al., 2020).

LncRNA DLX6-AS1 deficiency blocked tumor development due to inhibition of CADM1 promoter methylation and suppression of STAT3 pathway in liver CSCs (Wu D.-M. et al., 2019). Knockdown of DLX6-AS1 repressed spheroid formation and suppressed the expression of stem markers in liver CSCs, such as SOX2, Nanog, OCT4, CD13 and CD133 (Wu D.-M. et al., 2019). Similarly, DLX6-AS1 overexpression promoted stemness of osteosarcoma cells via interacting with miR-129-5p and activation of DLK1, leading to activating Wnt pathway (Zhang et al., 2018). Patients with high expression of DLX6-AS1 often had poor grade, advanced stage and poor overall survival (Zhang et al., 2018). Deficient of DLX6-AS1 decreased sphere size and number, and CD117+Stro-1+ cells were decreased in osteosarcoma cells after DLX6-AS1 silencing (Zhang et al., 2018).

LncRNA HIF2PUT was reported to regulate the proliferation, invasion and migration in osteosarcoma cells (Zhao D. et al., 2019). One group reported that HIF2PUT overexpression attenuated cell growth and motility in U2OS and MG-63 cells (Zhao D. et al., 2019). HIF2PUT expression was correlated with clinical features of osteosarcoma patients, including tumor size, stage, distant metastasis, and OS and DFS (Li W. et al., 2016). Interestingly, HIF2PUT was also reported to be highly expressed in osteosarcoma, suggesting that the deeper investigation is necessary to dissect the role of HIF2PUT in osteosarcoma tumorigenesis. HIF2PUT has been revealed to control CSCs in several types of human malignancies. For instance, HIF2PUT overexpression repressed CSC properties via targeting HIF-2α in colon cancer (Yao et al., 2015). Downregulation of HIF2PUT decreased the expression of stemness biomarkers in colon cancer DLD-1 and HT29 cells, leading to blockade of spheroid formation (Yao et al., 2015). However, downregulation of HIF2PUT elevated cell growth and migratory ability in MG63 cells, and elevation of HIF2PUT showed an opposite effect in osteosarcoma cells (Wang et al., 2015). Moreover, increased HIF2PUT led to a reduction of CD133 + MG63 cells and inhibition of sphere-forming ability, while decreased HIF2PUT resulted in an induction of CD133 positive cells and promotion of sphere-forming capacity (Wang et al., 2015). Another study validated that HIF2PUT upregulation inhibited sphere formation of osteosarcoma cells (Zhao D. et al., 2019). A mechanistical experiment showed that HIF2PUT could target HIF-2α expression and perform its biological function in osteosarcoma cells (Wang et al., 2015). Furthermore, the clinical data revealed that HIF2PUT expression was linked to HIF-2α levels in tumor tissues of osteosarcoma patients (Wang et al., 2015; Li W. et al., 2016).

LncRNA THOR was found to involve in CSC maintenance in TNBC cells (Wang B. et al., 2020). THOR expression was higher in TNBC tissues than that in luminal A-type and luminal B-type breast cancer (Wang B. et al., 2020). Silencing of lncRNA THOR attenuated the expression of stemness regulatory factors, including CD44, Nanog, and Oct4, and reduced ALDH1 activity, leading to suppressing the sphere-formation ability, which is evidenced by reduced sphere size and number in MDA-MB-231 and MDA-MB-453 cells (Wang B. et al., 2020). Overexpression of THOR promoted CSC properties and increased stemness factor expression, indicating that THOR might promote stemness of TNBC cells. Moreover, THOR interacted with β-catenin mRNA and increased its mRNA stability and elevated its expression (Wang B. et al., 2020). In line with the role of THOR in regulating CSCs, Cheng et al. found that THOR promoted CSC expansion and stimulated the self-renewal ability via targeting β-catenin axis in hepatocellular carcinoma (Cheng et al., 2019). Similarly, THOR knockdown reduced the stemness via inhibition of multiple stemness markers, such as CD44, SOX2, SOX9, Nanog, Oct1/2/4, and ALDH, in MKN-45 and BGC-23 gastric cancer cells (Song et al., 2018). Silencing of THOR attenuated the spheroids size and number and reduced the ability of spheroid formation in gastric cancer (Song et al., 2018). Moreover, depletion of THOR reduced SOX9 expression via binding to and increasing SOX9 mRNA stability (Song et al., 2018). In nasopharyngeal carcinoma (NPC) cells, THOR decreased sensitivity of cisplatin via promoting CSC stemness (Gao et al., 2018). THOR interacted with YAP and blocked its translocation to cytoplasm from nuclear, leading to enhancement of YAP transcription activity in NPC cells (Gao et al., 2018). In osteosarcoma cells, THOR increased stemness and migratory capacity via increasing stability of SOX9 mRNA (Wu H. et al., 2019). THOR expression was higher in cell spheroids than that in adherent cells in osteosarcoma. Upregulation of THOR elevated the ALDH activity and enhanced spheroid formation in adherent cells of osteosarcoma, whereas downregulation of THOR showed an opposite function in spheroids (Wu H. et al., 2019). THOR promoted osteosarcoma CSC stemness via increasing SOX9 mRNA stability and upregulating its expression (Wu H. et al., 2019). Altogether, lncRNA THOR participate in controlling CSCs in osteosarcoma.

LncRNA FER1L4 plays an anti-tumor role in osteosarcoma development (Fei et al., 2018). The evidence is that lncRNA FER1L4 has a lower expression in tissues of osteosarcoma patients, which is linked to stage and metastasis (Chen ZX. et al., 2018; Ye et al., 2019). In addition, FER1L4 retarded osteosarcoma tumorigenesis via sponging miR-18a-5p and increasing PTEN expression (Fei et al., 2018). FER1L4 was reported to control PDLSCs under compressive stress (Huang et al., 2019). One study found that 72 lncRNAs were increased and 18 lncRNAs were decreased in PDLSCs after static compressive stress (Huang et al., 2019). These lncRNAs contained FER1L4, NEAT1, LUCAT1 and HIF1A-AS2 (Huang et al., 2019). Moreover, FER1L4 stimulated osteogenic differentiation of PDLSCs via binding with miR-874-3p and targeting VEGFA, suggesting that FER1L4 could enhance bone formation (Huang et al., 2020). Furthermore, FER1L4 triggered the autophagy via regulating Akt/FOXO3 signaling pathway in PDLSCs under orthodontic compressive strain (Huang et al., 2021). Ma et al. reported that ectopic expression of FER1L4 inhibited proliferation, induced apoptosis, blocked migration and invasion, suppressed EMT in osteosarcoma cells (Ma L. et al., 2019). Moreover, silencing of FER1L4 upregulated the expression of several stemness biomarkers, including CD44, Oct4, SOX9, Nanog, and ALDH1 (Ma L. et al., 2019). In mechanism, FER1L4 suppressed tumor progression via targeting PI3K/Akt pathway in osteosarcoma.

One group showed that metastatic osteosarcoma patients had a higher level of LINK-A in plasma (Zhao B. et al., 2019). Elevation of LINK-A enlarged migratory and invasive capacity of osteosarcoma cells via induction of HIF-1α expression (Zhao B. et al., 2019). Another group also observed that LINK-A in plasma was highly expressed in osteosarcoma patients (Kong et al., 2020). LINK-A upregulation increased TGF-β1 expression in osteosarcoma cells. Deficient of LINK-A led to suppression of migration and invasion of osteosarcoma cells. Moreover, depletion of LINK-A decreased the percentage of CD133 + cells in osteosarcoma cell lines (Kong et al., 2020). This finding indicated that LINK-A might participate in governing stemness of osteosarcoma.

LncRNA MALAT1 has been discovered to regulate stem cell expression in osteosarcoma (Chen Y. et al., 2018). Chen et al. reported that MALAT1 expression level was increased in tumor tissues and linked to tumor size, metastasis and poor survival in osteosarcoma patients (Chen Y. et al., 2018). Ectopic expression of MALAT1 increased proliferation, migratory and invasive ability in osteosarcoma cells and promoted tumor growth in mice via sponging miR-129-5p and regulating the RET-Akt pathway (Chen Y. et al., 2018). It has been known that CD90, SOX2 and CD133 are well-characterized stemness markers. Moreover, MALAT1 upregulation elevated the expression of CD90, SOX2 and CD133 in SW1353 and SOSP-9607 cells. In consistent, depletion of MALAT1 reduced the expression of CD90, CD133 and SOX2 in osteosarcoma cells (Chen Y. et al., 2018). In line with this finding, MALAT1 overexpression in SW1353 and SOSP-9607 cells resulted in enhancement of CD133 + CD44 ⁺ cell proportion, while depletion of MALAT1 displayed the opposite effects (Chen Y. et al., 2018). This study suggested that MALAT1 enhanced stem cell-like features via promotion of RET expression via targeting miR-129-5p and subsequently activating the PI3K-Akt pathway in osteosarcoma. MALAT1 was highly expressed in patients with osteosarcoma (Wang et al., 2017c). MALAT1 promoted proliferation and metastasis via sponging miR-144-3p and blocking ROCK1/ROCK2 axis in osteosarcoma cells (Wang et al., 2017c).

LncRNA SOX2-OT has been characterized as an oncogene and is highly expressed in various cancers (Li PY. et al., 2020). Higher level of lncRNA SOX2-OT was existed in several osteosarcoma cell lines and tumor specimens. Notably, osteosarcoma patients with high level of lncRNA SOX2-OT often have bigger tumor size, advanced stage, high grade and metastasis and poor OS (Wang Z. et al., 2017). An in vitro experiment showed that knockdown of lncRNA SOX2-OT attenuated proliferation and migration and invasion of U2OS cells. In consistent, elevation of lncRNA SOX2-OT enhanced proliferation and facilitated invasive and migratory capacity in SaOS-2 cells (Wang Z. et al., 2017). Moreover, SOX2 was confirmed as a downstream target of lncRNA SOX2-OT in osteosarcoma. Strikingly, the expression of stemness biomarkers was downregulated in osteosarcoma cells after lncRNA SOX2-OT knockdown, including ALDH1, Nanog, Oct4, CD44 and CD133 (Wang Z. et al., 2017). Taken together, lncRNA SOX2-OT might regulate CSCs via positively regulating SOX2 in osteosarcoma.

B4GALT1-AS1 has been reported to serve as a ceRNA to sequester the expression of miR-30e, resulting in the upregulation of SOX9 in NSCLC (Lin et al., 2020). B4GALT1-AS1 had an increased expression in NSCLC tissues and cells. Silencing of B4GALT1-AS1 blocked malignant phenotype in A549 and H1299 cells, including cell viability and colony-forming ability (Lin et al., 2020). Deficient of B4GALT1-AS1 reduced clone formation capacity in colon cancer cells, and attenuated the expression of the stemness biomarkers. B4GALT1-AS1 silencing also reduced ALDH1 activity and retarded spheroid formation in colon cancer cells (Wu D.-M. et al., 2019). Mechanistically, B4GALT1-AS1 might enhance the relocation of YAP into nucleus from cytoplasm and promote its transcription, leading to maintenance of CSCs in colon cancer (Wu D.-M. et al., 2019). Similarly, higher expression of B4GALT1-AS1 was observed in osteosarcoma tissues. Depletion of B4GALT1-AS1 decreased proliferation and migratory capacity of osteosarcoma cells, blocked EMT progression, evidenced by an increase of E-cadherin and a decrease of vimentin (Li et al., 2018). Knockdown of B4GALT1-AS1 attenuated the expression of Nanog and ALDH1 and reduced the capability of spheroid formation, suggesting that B4GALT1-AS1 is involved in regulation of osteosarcoma cell stemness (Li et al., 2018). In vivo data further confirmed that B4GALT1-AS1 silencing decreased tumor formation in mice. B4GALT1-AS1 promoted the translocation of HuR into cytoplasm from nuclear and led to upregulation of YAP transcription in osteosarcoma (Li et al., 2018). Notably, deficient of B4GALT1-AS1 reduced adriamycin resistance in a YAP-dependent manner in osteosarcoma cells. This study revealed that B4GALT1-AS1 shed light on the regulation of CSC features in osteosarcoma.