Skip to main content
. 2025 Apr 24;13:e19332. doi: 10.7717/peerj.19332

Table 1. Mechanism of anti-tumor action of TCM monomers.

Classify TCM monomers Chemical formula of TCM monomers Source Experimental model Changes in tumor cells and tumors Antitumor mechanisms References
Steroid Bufalin graphic file with name peerj-13-19332-i001.jpg Bufo gargarizans Human gallbladder cancer cell lines GBC-SD and SGC-996 cells and Nude mice model with subcutaneous GBC-SD cell xenografts Inhibited cell proliferation, induced apoptosis and cell cycle arrest, reduced tumor volume by 40% Bufalin inhibits c-Met-mediated MEK/ERK and PI3K/AKT signaling pathways, suppressing tumor cell invasion, migration, and self-renewal of cancer stem cells. Bufalin (2 mg/kg) significantly reduced tumor volume by about 40% and effectively inhibited the growth of gallbladder cancer cells. (Qian et al., 2020)
Organic acids Betulinic acid graphic file with name peerj-13-19332-i002.jpg Betula platyphylla Suk GBC-SD and SGC-996 cells, Nude mice model with subcutaneous GBC-SD cell xenografts Inhibited cell migration and clonogenic ability Derivative Q-4 of betulinic acid induces apoptosis, autophagy, and cell cycle arrest, producing reactive oxygen species. Q-4 exerts anti-tumor effects by inhibiting the PI3K/AKT/mTOR signaling pathway and reversing trastuzumab resistance. (Cai, 2023)
Phenylpropanoid Verbascoside graphic file with name peerj-13-19332-i003.jpg Cistanche deserticola MCF-7, Hela, and MDA-MB-231 cells Significantly inhibited proliferation, migration, and invasion of GBM cells, promoted apoptosis and autophagy. Tumor volume was significantly reduced compared to the control group. Verbascoside significantly inhibits the proliferation, invasion, and migration of colorectal cancer cells by inhibiting the Ras-related C3 botulinum toxin substrate 1 (Rac-1), hypoxia-inducible factor-1α (HIF-1α), and zinc finger E-box binding homeobox 1 (Zeb-1) signaling pathways. (Jia et al., 2020)
Quinones Shikonin graphic file with name peerj-13-19332-i004.jpg Lithospermum erythrorhizon Hs683 cells Induced and promoted apoptosis Promoted apoptosis by activating Caspase-3 and upregulating PERK/CHOP protein levels. (Ma et al., 2020)
Phenols Emodin graphic file with name peerj-13-19332-i005.jpg Reynoutria japonica HaCaT cells Regulated cell cycle, promoted apoptosis Insulin growth factor receptor (IGF1R) is the key target of emodin in the treatment of gastric cancer. Emodin induces apoptosis of gastric cancer cells and inhibits proliferation by inhibiting the IGF1R/PDK1 signaling pathway. (Deng et al., 2023a)
Saponin Ginsenoside Rg3 graphic file with name peerj-13-19332-i006.jpg Panax ginseng NSCLC cell lines H1975, H1299, A549, HCC827 and LLC cell xenograft model Inhibited tumor growth, reduced tumor volume Rg3 inhibited the glycosylation of PD-L1 by suppressing the EGFR signaling pathway, thereby enhancing T cell-mediated anti-tumor immune responses. In vivo experiments showed that Rg3 dose-dependently increased the concentration of IL-2, IFN-γ, and TNF-α in mouse serum, while promoting the activation of CD8+ T cells in the tumor microenvironment, as evidenced by increased expression levels of perforin and granzyme B. (Wang et al., 2024a)
Terpenes Paclitaxel graphic file with name peerj-13-19332-i007.jpg Taxus brevifolia MDA-MB-231, Cal51, MCF10A and LLC cell xenograft model in C57/BL6J mice Enhanced cytotoxicity, reduced tumor volume Increasing the duration of multipolar spindle formation significantly enhanced the cytotoxicity of paclitaxel. Inhibiting Mps1 or upregulating Mad1 reduced the efficacy of paclitaxel. Mad1-upregulated MDA-MB-231 cells exhibited lower sensitivity to paclitaxel, with less tumor reduction compared to the control group. Paclitaxel exerts anti-tumor effects by inducing multipolar spindle formation and chromosomal instability. (Scribano et al., 2021)
Alkaloids Berberine graphic file with name peerj-13-19332-i008.jpg Coptis chinensisFranch HT-29 colorectal cancer cells and CRC mouse model Inhibited proliferation, migration, invasion, and clonogenic ability of HT-29 cells, induced apoptosis Berberine concentration- and time-dependently reduced the levels of anti-apoptotic protein Bcl-2, upregulated pro-apoptotic protein Bax expression, and activated Caspase-9 and Caspase-3. By inhibiting the abnormal activation of the Hedgehog signaling pathway, it reduced the expression of SHH, Ptch1, SMO, Gli1, and c-Myc, while enhancing the expression of SUFU, thereby suppressing the malignant phenotype of CRC cells. In vivo experiments showed that berberine significantly alleviated the pathological features of AOM/DSS-induced CRC mice, increased survival rates, relieved colon shortening, and reduced the activity of the Hedgehog signaling pathway. (Sun et al., 2022)
Flavonoids Puerarin graphic file with name peerj-13-19332-i009.jpg Rutagravolelensl PANC-1 and PATU-8988T cell lines, nude mice model with subcutaneous xenografts Inhibited cell proliferation, induced mitochondria-mediated apoptosis, reduced tumor mass and volume Bax/Bcl-2 imbalance, puerarin concentration- and time-dependently inhibited epithelial-mesenchymal transition (EMT) to suppress cell migration and invasion. Puerarin reduced Ki67 and c-Myc expression, upregulated Cleaved caspase-8 and Bax, downregulated Bcl-2 expression, while inhibiting the expression of EMT-related protein α-SMA and increasing E-cadherin expression. (Zhu et al., 2021)