Terpenoids are essential constituents of natural organic compounds, with over 50,000 reported varieties. Natural terpenoids exhibit potent anti-tumor, anti-inflammatory, and antibacterial activities. These include sesquiterpenoids, diterpenoids, monoterpenoids, disesquiterpenoids, and triterpenoids that contain one or more carbon atoms with double or triple bonds. They are widely distributed in plants, microorganisms, marine organisms, and certain insects (Liyuan et al., 2024).

The artemisinin, derived from the Chinese herb Artemisia caruifolia Buch.-Ham. ex Roxb. (Ma et al., 2020). Some studies have demonstrated that the expression of relevant genes and proteins was assessed using RT-qPCR and Western blot analysis with a concentration of 300 μM artemisinin. The findings revealed a significant downregulation of ERa and VEGF expression by artemisinin, thereby further confirming its potential anti-angiogenic effect in cervical cancer cells. Moreover, artemisinin reduced telomerase activity, hTR and hTERT subunits, as well as the expression of HPV-39 virus E6 and E7 components, while increasing p53 expression. These results provide additional evidence supporting the reliance on p53 for artemisinin-induced apoptosis. Overall, these findings suggest that artemisinin exerts anti-proliferative and pro-apoptotic effects in HPV-39-infected ME-180 cells. However, the lack of an in vivo experiment and absence of a positive control group in this study preclude confirmation of artemisinin’s superiority (Teodoro et al., 2007; Mondal and Chatterji, 2015).

The semi-synthetic derivative of artemisinin, known as artesunate (ART), exhibits superior efficacy as an antimalarial drug compared to artemisinin (Moore et al., 1995; Efferth et al., 2001; Wu et al., 2001; Efferth et al., 2002). Through in vivo and in vitro studies, ART shows promise as an effective inhibitor of angiogenesis. Human ovarian cancer HO-8910 cells were implanted into nude mice, and four groups were established: a control group and ART high, medium, and low dose groups (10, 50, and 100 mg/kg). Subcutaneous injections of ART were administered daily. After 15 days of treatment, the tumors were removed and immunohistochemistry was performed to detect CD31 expression as well as VEGF levels and VEGF receptor KDR/flk-1 expression. It was observed that the expression of these markers decreased following drug treatment, resulting in slowed tumor growth and reduced microvascular density. Furthermore, no evident toxicity to animals was observed. The angiogenesis model using HUVEC cells was also tested. The results demonstrated that ART significantly suppressed VEGF expression on HO-8910 cells as well as KDR/flk-1 expression on both HUVEC cells and HO-8910 cells. Moreover, ART exhibited a dose-dependent inhibition of angiogenesis within the range of 0.5–50 μmol/L (Chen et al., 2004).

Betulin, an essential compound derived from the bark of Betula pendula subsp. mandshurica (Regel) Ashburner & McAll., can be converted into betulinic acid. Dehelean et al. (2012) investigated the cytotoxic effects of betulin (3, 10, 30 μM) on HeLa, MCF7, and A431 cancer cells and elucidated the underlying apoptotic mechanism. Additionally, they explored the correlation between betulin and angiogenesis in the chorioallantoic membrane of chicken embryos. The results demonstrated that betulin exhibited a superior inhibitory effect on cervical cancer cells. At higher concentrations, betulin induced cell membrane disruption, thereby sustaining its apoptotic impact. Betulin prompted a reduction in neovascularization and appeared to function as a drug targeting vascular endothelial cells, potentially through apoptosis-mediated mechanisms, leading to diminished functional blood vessels within the rapidly proliferating capillary cluster in the chorio-allantoic membrane of chicken embryos. These findings underscored the significant dose-dependent anti-tumor and anti-angiogenic activities of betulin. However, there are certain limitations in the experimental design such as the absence of a positive control group and limited relevant detection indicators; thus further verification is required to ensure the reliability of these experimental outcomes.

Ginsenoside Rg3, a monomeric compound extracted from Panax ginseng C.A.Mey., is a trace element in traditional Chinese medicine that has been shown to inhibit the adhesion, invasion, and proliferation of tumor cells as well as the formation of tumor neovascularization. The cervical cancer-bearing nude mouse model was treated with ginsenoside Rg3 (5 mg/kg) via oral gavage for a duration of 5 weeks. Both a cisplatin positive control group and a combined treatment group were established. Immunohistochemical analysis was conducted to determine the expression of CD31 and PCNA in tumor tissues, while apoptosis was assessed using the TUNEL method. The results demonstrated that ginsenoside Rg3, either alone or in combination with cisplatin, effectively inhibited the growth of Hela cell transplanted tumors in nude mice. Furthermore, it downregulated the expression of CD31 and PCNA, thereby inhibiting angiogenesis in cervical cancer. Additionally, it enhanced the drug sensitivity of cisplatin towards cervical cancer cells and mitigated its associated side effects (Yingchun, 2007) Moreover, a study established an abdominal cavity transplantation tumor model of severe combined immunodeficiency (SCID) mice with ovarian cancer and divided them into three groups: blank group, control group, and experimental group (ginsenoside Rg3, 0.75 mg/mL), which underwent continuous gavage treatment for 26 days. VEGF mRNA, protein expression, and microvascular density (MVD) were assessed through reverse transcription polymerase chain reaction, enzyme-linked immunosorbent assay, and immunohistochemistry respectively. The findings revealed that ginsenoside Rg3 suppressed tumor growth and metastasis by down-regulating VEGF mRNA and protein expression (Zimin et al., 2002). However, pharmacological toxicity or clinical-related experimental studies were not conducted in these two experiments; hence the safety profile and clinical therapeutic effect require further investigation.

Additionally, we have identified a variety of terpenoid compounds (Supplementary Table S1), which also play a significant role in the treatment of gynecological cancers.

Anthraquinone compounds are naturally present in various plant families, including polygonaceae, rhamnaceae, rubiaceae, legumes, scrophulariaceae, liliaceae. They can also be found in small amounts in lichens, fungi and animal metabolites. These compounds exhibit antibacterial, anti-inflammatory, antiviral and antioxidant effects. Moreover, they have the ability to influence tumor cell proliferation and differentiation as well as induce tumor cell decay. Additionally, they can reverse multidrug resistance (NMR) associated with malignant tumors. Natural anthraquinones come in a variety of forms with distinct structures and pharmacological activities (Mingming et al., 2019).

The impact of emodin on the proliferation of U14 cervical cancer cells transplanted in mice was investigated by several scholars (Zhang et al., 2015). The mice were divided into four groups: a control group (treated with DMSO), a low-dose emodin group (20 mg/kg), a high-dose emodin group (40 mg/kg), and a cisplatin group (3 mg/kg). They received oral administration for 26 days. MVD was assessed using immunohistochemistry. Real-time quantitative RT-qPCR and Western blot were employed to analyze the mRNA and protein levels of HIF-1α, VEGF, and MIF, respectively. Results showed that CD34, HIF-1α, VEGF, MIF, and Bcl-2 levels significantly decreased while Bax levels significantly increased following treatment with emodin. These findings suggest that emodin may inhibit cervical cancer in mice by suppressing tumor neovascularization, reducing MIF expression, and promoting tumor cell apoptosis. The experiment solely focused on in vivo studies, without conducting any in vitro experimental studies to enhance the experimental design and validate the data’s reliability.

The bioactive compound dihydrotanshinone I (DHT) is present in Salvia miltiorrhiza Bunge. DHT exhibits the ability to deactivate the NF-κB signaling pathway, thereby suppressing the expression of COX-2, MMP-9, and VEGF. Consequently, it effectively inhibits tumor cell invasion and angiogenesis (Wang et al., 2015). The in vitro experiments demonstrated that DHT effectively dose-dependently inhibited the expression of the NF-κB reporter gene induced by TNF-α. Moreover, it inhibited the phosphorylation and degradation of IκBα, as well as the phosphorylation and nuclear translocation of p65. Additionally, DHT downregulated the expression levels of cIAP-1, FLIP, COX-2, MMP-9, VEGF, TNF-α, IL-6 and MCP1. Furthermore, DHT significantly impeded the activation of ERK1/2, p38 and JNK/SAPK. The in vivo studies have demonstrated that DHT effectively suppresses the growth of HeLa cells in xenograft tumor models, potentially through its regulation of TNF-α production. The summary indicates that DHT has demonstrated the ability to inhibit NF-κB and its regulatory gene products, which are associated with various beneficial effects including anti-proliferative, pro-apoptotic, anti-invasive, anti-angiogenic, and anti-inflammatory properties (Wang et al., 2015). The lack of a positive control group in this experiment unfortunately undermines its credibility to some extent.

The anti-proliferative effects of Nigella sativa L. (NS) seed ethanol extract and its volatile oil thymoquinone (THM) on SKOV3 cells were investigated at varying drug concentrations (4μM, 4μM, 100μM, and 100 μM), with the drug concentration adjusted to NS (50 μg)/THM (50 μM) based on IC50. After a 24-h intervention in SKOV3 cells, Western blot was used to detect the expression levels of related proteins. Results in comparison to the control group, docetaxel (DTX), paclitaxel (PTX), NS, THM, and DTX/PTX + NS/THM significantly induced elevated levels of IL-8 and pro-apoptotic protein Bax. Conversely, the expression of TNF-α, VEGF, and Bcl-2 protein was downregulated. The anti-proliferative, anti-angiogenic, and pro-apoptotic activities exhibited by NS and THM clearly demonstrate their potential in combating ovarian cancer. NS and THM alone or in combination with DTX and PTX inhibit SKOV3 growth through pathways mediated by IL-8, TNF-α, VEGF as well as Bax/Bcl-2 (Mathur and Tiwari, 2016). Although the study confirmed the anticancer effects of NS and THM in ovarian cancer, further verification is necessary due to the lack of in vivo experiments and unclear identification of therapeutic components within the NS ethanol extract.

Glycosides are natural products synthesized from various plants, possessing pharmacological properties such as anti-inflammatory, anti-tumor, anti-oxidative, anti-fibrotic, anti-allergic, antidiabetic, antidepressant and antifungal effects. Additionally, they enhance the body’s immunity and have cardioprotective and neuroprotective effects by dilating blood vessels and preventing arrhythmia (Xingwen et al., 2023).

The securidaca saponin was isolated from a purified root extract of Securidaca longepedunculata Fresen. Previous studies have identified the main components extracted from the plant (4A3 and 4A4) as triterpenoid glycosides (Obasi et al., 2018). Treatment with 4A3 and 4A4 at concentrations of 7.03 and 16.39 μg/mL respectively significantly attenuated cell migration in Caski and Bu25 TK cells after both 48 h and 72 h of exposure. The RT-qPCR analysis revealed that the expression of MCL-1, BCL2L1, AKT-3, VEGFA, and MALAT1 was downregulated through modulation of the PI3K-AKT/mTOR/NF-κB signaling pathway. The findings demonstrated that 4A3 and 4A4 effectively suppressed cancer cell proliferation, induced apoptosis, inhibited angiogenesis, and hindered cervical cancer cell survival through diverse mechanisms (Obasi et al., 2018). The experiment, however, also revealed certain limitations as it did not include in vivo experimentation and lacked a positive control group. Therefore, further verification is required to ensure the reliability of the experimental data.

Teasaponin E₁ (TSE₁) is an oleanane-type saponin derived from the seeds of Camellia sinensis (L.) Kuntze. Li et al. (2021) conducted in vitro experiments and chicken chorio-allantoic membrane (CAM) experiments to investigate the apoptosis-inducing, cell cycle arrest, and anti-angiogenesis activities of TSE₁ on platinum-resistant ovarian cancer cells. The results demonstrated that TSE₁ effectively suppressed the growth of ovarian OVCAR-3 and A2780/CP70 cells in a concentration-dependent manner while exhibiting minimal toxicity towards normal ovarian IOSE-364 cells. In this experiment, They established the Control group, TSE₁ group (2 µM), Akt signaling inhibitor (wortmannin) group (100 nM), Notch1 signaling inhibitor (DAPT) group (80 µM), as well as the TSE₁+ DAPT/wortmannin groups. The results demonstrated that TSE₁ effectively induced apoptosis in OVCAR-3 cells through both endogenous and exogenous apoptotic pathways. Additionally, it modestly arrested the cell cycle at the G2/M phase and significantly suppressed OVCAR-3 cell proliferation by downregulating the protein expression of VEGF, HIF-1α, 4E-BP1, NICD, Dll4, and Jagged1. Moreover, TSE₁ exhibited inhibitory effects on migration and angiogenesis. To evaluate its antiangiogenic activity in vivo, we employed the CAM assay. Compared to the control group (TSE₁ with a drug concentration of 4 µM), TSE₁ remarkably reduced both the number and density of CAM vessels. In summary, the TSE₁ may potentially enhance the treatment of platinum-resistant ovarian cancer through modulation of the Dll4/Jagged1-Notch1-Akt-HIF-1α signaling pathway. However, the absence of a drug-positive control group in this experiment, compromised the study’s reliability. Additionally, another experimental study demonstrated the potent anti-proliferative effects of TSE₁ on OVCAR-3 and A2780/CP70 ovarian cancer cells. Furthermore, TSE₁ appears to induce apoptosis in human ovarian cancer cells via an exogenous pathway and reduce VEGF protein levels through an HIF-1α-dependent mechanism, thereby effectively inhibiting angiogenesis in these cells (Jia et al., 2017).

Alkaloids are a class of significant natural bioactive compounds in traditional Chinese medicine. They are organic nitrogen-containing compounds that occur naturally, primarily in plants with a few originating from animals. Possessing intricate ring structures and predominantly alkaline properties, they exhibit diverse functionalities including analgesic, antibacterial, anti-inflammatory effects as well as cough and asthma relief and anticancer activities (Lu et al., 2022).

Sanguinarine is widely distributed in nature and derived from Macleaya cordata (Willd.) R. Br. Its primary constituents belong to the isoquinoline alkaloids. Through in vitro cell experiments, Jiaying (2013). discovered that sanguinarine exhibits concentration- and time-dependent inhibition on the adhesion, migration, movement, invasion, and metastasis of HeLa and Siha cells derived from cervical cancer. Moreover, it significantly suppresses cell invasion and metastasis at non-toxic doses. The underlying mechanism involves upregulation of E-cadherin and PTEN protein expression levels while downregulating α-catenin, β-catenin, γ-catenin, MMP-2, MMP-9, and VEGF expression levels. In the in vitro study, a total of 40 nude mice were divided into four groups: normal saline control group, cisplatin positive control group (5 mg/kg), sanguinarine low concentration group (1.25 mg/kg), and sanguinarine high concentration group (2.5 mg/kg). The mice were treated for a duration of 28 days. Immunohistochemistry, Western blot analysis, and transmission electron microscopy techniques were employed to evaluate the effects. The findings revealed that treatment with hemagglutinine resulted in downregulation of CD34, Ki67, EGFR, Bcl-2, and VEGF expressions in tumor tissues while up-regulating the pro-apoptotic protein Bax expression. These results indicate that sanguinarine possesses inhibitory properties against xenografted cervical cancer growth in vivo by exerting anti-angiogenic effects, suppressing tumor cell proliferation, inducing apoptosis and autophagy mechanisms. Although the experimental design was relatively comprehensive, one limitation was the absence of a positive control group in the cell experiment.

Crinamine is primarily derived from the bulbs of Crinum asiaticum L. Khumkhrong et al. (2019) demonstrated, for the first time, the mechanism of action of crinamine in inhibiting cervical cancer. It exhibits superior inhibition of unanchored tumor sphere growth compared to existing chemotherapy agents carboplatin and 5-fluorouracil or CDK9 inhibitor FIT-039. Crinamine induces cell apoptosis without promoting DNA double strand breaks and suppresses cervical cancer cell migration by downregulating SNAI1 and VIM expression, positive regulators of epithelial-mesenchymal transition. Notably, crinamine also exerts anti-angiogenic activity by inhibiting VEGFA protein secretion and vascular development in zebrafish embryonic cervical cancer cells. Gene expression analysis suggests that its mechanism of action may involve downregulation of cancer-related genes such as AKT1, BCL2L1, CCND1, CDK4, PLK1, and RHOA.

The study conducted by Tran et al. (2022). extracted oxostephanine from the leaves of Stephania dielsiana Y.C.Wu., and demonstrated its potential as an aurora kinase inhibitor. A comparison was made between oxostephine and the aurora kinase inhibitor VX-680 in terms of their effects on OVCAR-8 cell growth in ovarian cancer. The results revealed that oxostephine effectively inhibited the growth and migration of OVCAR-8 cells, while selectively exhibiting cytotoxicity towards HUVEC but demonstrating lower toxicity towards hFBs cells. Furthermore, oxostephine downregulated the expression of VEGFA, HGF, and FG2 in both HUVEC and hFBs cells, indicating its role in regulating cell proliferation, migration, and angiogenesis. In conclusion, a limited number of aurora kinase inhibitors have been identified and developed for clinical trials in cancer treatment with some degree of efficacy observed. However, further testing is required to evaluate the impact of oxostephine on other ovarian cancer cell lines, particularly primary cell lines to validate its effectiveness against ovarian cancer. Moreover, it is crucial to conduct in vivo tumor model experiments to confirm the inhibitory effects of oxostephine on both auroral kinase activity and angiogenesis.

Polyphenol compounds are secondary metabolites synthesized by plant tissues, characterized by the presence of multiple phenolic groups. They are widely distributed in various plant-based foods and can be derived from a variety of fruits, vegetables, tea, coffee, wine, and whole wheat products (Fengxia and Zeli, 2023; Yaru and Wentao, 2023).

The phenolic compound curcumin (CUR) extracted from Curcuma longa L. has been demonstrated in numerous recent studies to exert regulatory effects on angiogenesis, proliferation, invasion, and tumor progression across various cancer types. Yoysungnoen-Chintana et al. (2014) discovered thatm CUR effectively inhibited tumor progression and angiogenesis in nude mice transplanted with cervical cancer cells (CaSki-). A total of 36 nude mice were divided into six groups: Control + vehicle (corn oil); Control + CUR (1,500 mg/kg); CaSki + vehicle (corn oil); CaSki + CUR (500 mg/kg); CaSki + CUR (1,000 mg/kg); CaSki + CUR (1,500 mg/kg) for a duration of 30 days. The immunohistochemical analysis revealed a significant reduction in the expression levels of CD31, VEGF, COX-2, and EGFR. In conclusion, the high-dose administration of CUR demonstrated its potential to suppress tumor growth and angiogenesis in caski-transplanted mice through the downregulation of VEGF, COX-2, and EGFR signaling pathways. Although this experiment confirmed the anti-cervical cancer effect of CUR, the absence of a positive control group and the omission of any experimental study on pharmacological toxicity raise concerns regarding safety and call for further verification of the reliability of experimental data.

Tetrahydrocurcumin (THC) is a significant metabolite of CUR in vivo. Research has demonstrated that THC exhibits more potent anti-angiogenesis activity against tumors compared to CUR (Yoysungnoen et al., 2008), which may be attributed to its higher antioxidant activity. Female BALB/c nude mice were divided into a control group and a CaSki group, with daily oral administration of CUR 100, 300, and 500 mg/kg for 30 days. MVD was assessed by CD31 expression, while the expressions of VEGF, VEGFR-2 and HIF-1 were detected through immunohistochemistry. The MVD in the CaSki + loading group was significantly higher than that in the CON + loading group; however, treatment with high, medium and low doses of THC resulted in a significant reduction in MVD among the CaSki group. Furthermore, while expressions of VEGF, VEGFR-2 and HIF-1 were significantly increased in the CaSki + loading group compared to controls without intervention; these expressions were downregulated by THC intervention. Thus suggesting that THC can inhibit tumor angiogenesis in caski transplanted nude mice via downregulation of HIF-1α and VEGF as well as its receptor’s expression levels (Yoysungnoen et al., 2015). It is important to note that this experiment did not include a positive control group nor conduct experimental studies related to pharmacological toxicity; therefore further verification is necessary.

EGCG (e)-epigallocatechin-3-gallate, a predominant polyphenol found in Camellia sinensis (L.) Kuntze, exhibits potent anticancer properties. Numerous studies have demonstrated the potent anti-cancer and cancer prevention effects of C. sinensis extract and EGCG in various human cancers (Yang, 1997; Sato, 1999; Lambert and Yang, 2003). Both C. sinensis extract and EGCG can effectively suppress the expression of HIF-1α and VEGF in HeLa cells through the PI3K/Akt and ERK1/2 signaling pathways, thereby inhibiting angiogenesis (Zhang et al., 2006). Another study demonstrated that EGCG can attenuate the expression of VEGF induced by basal and ET-1, as well as the activity of MMPs and uPA/uPA receptor, thereby inhibiting cell invasion. These findings suggest that EGCG’s suppression of the ET-1/ETAR autocrine loop may contribute to its anti-angiogenic and anti-invasive activities in ovarian cancer (Spinella et al., 2006). The absence of a positive control group in both trials precluded the determination of the effect. However, EGCG’s clinical application is limited due to poor bioavailability and the requirement for high doses to achieve therapeutic effects. The production of pro-polyphenol (−)-epigallocatechin-3-gallate (−) through acetylation of EGCG has been found to act as a prodrug, enhancing stability and bioavailability both in vitro and in vivo (Man et al., 2020).

The role of polyphenols in the prevention of gynecological cancer is significant, as evidenced by numerous additional compounds (Supplementary Table S1) with similar properties.

Flavonoids, as one of the three major secondary metabolites in plants, play crucial roles in plant growth and development, resistance to external adverse environments, and human nutrition and health. The flavonoid components are generally classified into seven categories: flavone, flavonol, isoflavone, flavanone, flavanol, anthocyanidin, and chalcone. The compounds exhibit a range of pharmacological effects, such as anti-inflammatory properties, antiviral activities, cardioprotective effects against heart diseases, anticancer properties, and anti-aging effects (Chao et al., 2023).

The flavonoid liquiritigenin (7,4′-dihydroxyflavanone, LQ), extracted from Glycyrrhiza glabra L., possesses antioxidant, anti-inflammatory, and anticancer properties (Kim et al., 2009; Kim et al., 2011). The cell survival rate was significantly reduced in a dose-time dependent manner when HUVEC and HeLa cells were treated with various concentrations of LQ (25, 50, 75, 100 μM). Western blot analysis revealed that LQ effectively inhibited the expression of VEGF and HIF-1α in both cell types, exhibiting a dose-dependent effect. Subsequent treatment with specific inhibitors including LY294002 (PI3K inhibitor), Rapamycin (p70S6K inhibitor), and U0126 (ERK1/2 inhibitor) resulted in downregulation of VEGF and HIF-1α expression mediated by the PI3K/AKT/p70S6K and ERK1/2 signaling pathways. These findings suggest that the inhibitory mechanism of LQ on HeLa cells may be associated with the PI3K/AKT/mTOR-p70S6K signaling pathway (Xie et al., 2012). Furthermore, research has demonstrated that LQ can downregulate the expression of HIF-1a and VEGF in human cervical cancer cells through the VEGF signaling pathway, thereby exerting an anti-angiogenic effec (Liu et al., 2012). The absence of a positive control group and the lack of animal experimental studies in both experiments necessitate further verification to ensure the reliability of the experimental data.

Formononetin, a naturally occurring isoflavone that can be extracted from Astragalus mongholicus Bunge, exhibits diverse biological functions including anti-inflammatory, antioxidant, and hepatoprotective effects (Zheng et al., 2020). The inhibitory effects of onononin on RAS/ERK and JAK1/STAT3 signaling pathways have been validated through in vitro and in vivo studies, leading to the regulation of STAT3, PD-L1, and MYC-related targets. Ultimately, this mechanism is the impediment of cervical cancer progression and angiogenesis (Wang et al., 2022). The trial lacked a positive control group, thus preventing the confirmation of formononetin’s superiority.

The flavonoid compound acacetin (5,7-dihydroxy-40-methoxyflavone) is commonly present in various plants, seeds, and flowers and exhibits anticancer properties. The OVCAR-3/A2780 cells were subjected to treatment with varying concentrations of acacetin (10, 20, 30 μM). RT-qPCR and Western blot analyses revealed that acacetin downregulated the expression of HIF-1a and AKT. The number of blood vessels was assessed through CAM experimentation, while the expressions of HIF-1 and VEGF were detected using Western blot and RT-qPCR techniques. The findings revealed a decrease in blood vessel count, as well as a reduction in HIF-1a and VEGF expression upon treatment with acacetin. In conclusion, acacetin hinders ovarian cancer progression and angiogenesis by suppressing VEGF expression via inhibition of the AKT/HIF-1 signaling pathway (Liu et al., 2011). Notably, the study lacked a positive control group and did not include any animal experiments.

Phenylpropanoids can be classified into various chemical categories, including simple phenylpropanols, coumarins and lignans. Coumarins is a natural product characterized by its aromatic nature and widespread occurrence in plants such as Apiaceae, Rutaceae, Asteraceae, legumes, orchids, among others. In recent years, coumarin-containing natural products have gained significant attention in clinical applications due to their remarkable therapeutic effects such as antioxidative, anti-tumoral, antibacterial, antiviral, anti-inflammatory properties as well as neuroprotective activities.

Angelol-A is a coumarin compound extracted from the root of Angelica pubescens. The study conducted by Ying et al. (2022), demonstrated the treatment of cervical cancer cells with varying concentrations of angelol-a (40, 80, 120 μM). Cell viability was assessed using the MTT assay, while cell cycle analysis was performed by PI staining. The expression of miR-29a-3p, in vitro migration/invasion, and angiogenesis were evaluated in angelol-a-treated cells with/without antago-miR-29a-3p (miR-29a-3p inhibitor) or U0126 (MEK inhibitor), using RT-qPCR for miR-29a-3p expression analysis, a chemotaxis assay for migration/invasion assessment, and a tube formation assay for angiogenesis evaluation. The expressions of MMP2, MMP9, and VEGFA were detected using Western blot analysis. It was observed that angelol-a significantly suppressed the expression of MMP2 and VEGFA, as well as inhibited cell migration and invasive behavior in human cervical cancer cells. Moreover, angelol-a exhibited inhibitory effects on invasion, motility, and angiogenesis by upregulating miR-29a-3p expression in the targeted vegf-3′utr region. These findings provide novel evidence for the anti-metastatic and anti-angiogenic properties of angelol-a in human cervical cancer cells through modulation of the ERK pathway and targeting the miR-29a-3p/MMP2/VEGFA axis.

However, the experiment had certain limitations and was not tested in vivo.

Honokiol, is a bioactive compound that is extracted from Magnolia officinalis Rehder & E.H.Wilson. and classified as a lignin compound, exhibits diverse pharmacological effects including antioxidation, anti-thrombosis, anti-inflammation, xanthine oxidase inhibition, anxiolytic properties, as well as antitumor activity. Li et al. (2008) investigated the in vitro and in vivo antitumor activity of Honokiol against human ovarian tumors. Cell proliferation and apoptosis were assessed using MTT, DNA ladder, Hoechst staining, and flow cytometry assays. The results demonstrated a dose- and time-dependent downregulation of Bcl-XL expression and upregulation of Bad expression. In the in vivo study, nude mice were randomly divided into three groups: Control group (PBS 100 mL), liposome group (0.6 mg/100 mL PBS), and Honokiol group (1 mg liposome-encapsulated honokiol [40%]/100 mL PBS). Intraperitoneal injections were administered daily for 56 days. The findings revealed that magnolol reduced VEGF and CD31 expression, decreased microvessel density, and inhibited tumor growth. These results suggest that Honokiol induces apoptosis and inhibits angiogenesis both in vitro and in vivo. It is worth noting that this experiment lacks a positive control group, thus further verification is required to ensure the reliability of the findings.

The most prevalent benzyls compound in liverwort is bisbibenzyl, which exhibits significant biological activities including antifungal, antimicrobial, antioxidant, and anti-platelet aggregation properties. Bibenzyl compounds are distinctive polyphenolic aromatic compounds found in bryophytes. Their remarkable biological activities have well-defined mechanisms and targets (Juan, 2013).

Erianin, derived from Dendrobium chrysotoxum Lindl., is a naturally occurring dibenzyl compound with antioxidant, anti-angiogenic, anti-tumor, antibacterial, antiviral, and other pharmacological effects (Kamory et al., 1995; Manfredi et al., 2001). The antitumor activity of erianin was evaluated by Yang et al. (2021), using an in vitro HeLa cell model and an in vivo cervical cancer xenotransplantation model. In the in vitro experiments, various concentrations of erianin (1, 3, 10, 30, and 100 μM) were administered to HeLa cells for durations of 12, 24, or 48 h. The impact of erianin on proteins, genes, and pathways associated with its antitumor activity was investigated through MTT assays, Western blot analysis, RT-qPCR analysis, and immunoprecipitation techniques, etc. Experimental findings demonstrated that erianin suppressed PD-L1 expression while promoting its lysosomal degradation; it also downregulated the expression levels of VEGF and MMP-9. Furthermore, erianin disrupted the interaction between RAS and HIF-1α. Notably, co-culture experiments involving T-cells and HeLa cells confirmed that erianin restored cytotoxic T lymphocytes’ ability to eliminate tumor cells. In the in vivo experiment, nude mice were randomly divided into four groups: the erianin low-dose group (25 mg/kg), high-dose group (75 mg/kg), 5-FU group (48 mg/kg), and control group. The treatment duration was 33 days in total. Western blot analysis of tumor tissues revealed that erianin concentration-dependently reduced the protein levels of PD-L1, HIF-1α, RAS, and VEGF, exhibiting a superior inhibitory effect compared to 5-FU. Furthermore, immunohistochemical analysis demonstrated that erianin significantly decreased the expression of PD-L1, HIF-1α, RAS, and VEGF when compared with the control group. Mechanistically, erianin inhibited HIF-1α synthesis through the mTOR/p70S6K/4EBP1 pathway and suppressed RAS/Raf/MEK/MAPK-ERK signaling cascade. Immunoprecipitation experiments indicated that erianin effectively hindered PD-L1-mediated angiogenesis as well as proliferation, invasion, and migration processes. Overall findings suggest that erianin modulates PD-L1 expression by preventing its interaction with HIF-1α while also exerting anti-tumor effects on angiogenesis and proliferation both in vivo and in vitro. The experimental design is relatively comprehensive and requires validation through clinical trials.

Indole compounds are widely present in nature, primarily found in natural floral oils such as jasmine, bitter orange flower, daffodils, and fragrant loran. They possess pharmacological properties including antipyretic and analgesic effects, hypotensive activity, vasodilation, and amine blocking inhibition.

Diindolylmethane (DIM), a phytonutrient and plant indole present in cruciferous vegetables such as broccoli, Brussels sprouts, cabbage, cauliflower, and kale, exhibits potential anti-androgenic and antineoplastic properties. Kandala et al. (2011) divided the cell test was divided into four groups: Control group, DIM group (50 μM), cisplatin group (10 μM), and DIM + cisplatin group. Western blot analysis revealed a significant 90% reduction in STAT-3 protein levels following combination therapy compared to individual treatment with cisplatin or DIM alone. Moreover, the expression of mcl-1 and survivin, which are regulated by STAT-3, was also downregulated. Additionally, there was a notable increase in caspase-3 and PARP cleavage. Furthermore, the results from the aortic ring assay exhibited complete inhibition of microvascular bud formation with combination treatment. In SKOV-3 cells, the combined administration of DIM and cisplatin resulted in a 50% decrease in VEGF secretion compared to only 20% inhibition observed with cisplatin alone. To summarize, DIM enhances the efficacy of cisplatin by blocking STAT-3 activation and inhibiting angiogenesis as well as metastasis. Unfortunately, the in vivo validation of the further mechanism underlying this combination therapy has not been conducted.

Melatonin is a biogenic amine present in animals, plants, and microorganisms. Yiqing et al. (2020) conducted an investigation to examine the impact of melatonin on invasion, migration, and angiogenesis of ovarian cancer cells both in vitro and in vivo. The effects of melatonin on the proliferation, invasion, and migration of SKOV3 cells were observed through MTT assay, scratch assay, and Transwell invasion assay respectively. HUVECs were induced to form tubes to evaluate the effect of melatonin on them. Western blot analysis was employed to assess the expression levels of VEGF, E-cadherin, MMP9, and Vimentin in SKOV3 cells. The results demonstrated that melatonin inhibited the invasion and migration abilities of ovarian cancer SKOV3 cells while up-regulating E-cadherin expression and down-regulating MMP-9, vimentin, and VEGF protein expressions. Furthermore, melatonin suppressed tubulogenesis in HUVECs. Immunohistochemistry was used to detect CD31 expression in ovarian cancer xenograft models which were randomly divided into two groups: Control group (200 μL normal saline) and MEL group (25 mg/kg) for 3 weeks. The results indicated a decrease in CD31 expression level, suggesting that melatonin could inhibit microvessel density. In conclusion, melatonin inhibits invasion, migration, and angiogenesis of ovarian cancer cells. The experimental design is relatively straightforward, lacking a positive control group, thereby compromising certain aspects of reliability.

Rapamycin, also known as Sirolimus, is a macrocyclic lactone antibiotic derived from the bacterium Streptomyces hygroscopicus. It was originally isolated from the soil of Rapa Nui (Easter Island) in the Vai Atari region. The ovarian cancer SKOV-3 cells were divided into four groups: blank control group, cisplatin group (10 μmol/L), rapamycin group (40 nmol/L), and combination group (10 μmol/L cisplatin +40 nmol/L rapamycin). Cell viability, ATP production, and VEGF content in the supernatant were measured. The results demonstrated that the MTT value, ATP content, and VEGF content of the cisplatin group, rapamycin group, and combination group were significantly lower than those of the blank control group. Moreover, the combination therapy exhibited superior effects. These findings suggest that rapamycin enhances the inhibitory effect of cisplatin on ATP production and angiogenesis in ovarian cancer SKOV-3 cells. Furthermore, a synergistic effect is observed when both drugs are used together (Zhonghua, 2015). However, it should be noted that this experiment lacks certain credibility due to the absence of concentration gradient comparisons and in vivo animal experiments.