Table 2.
Regulatory effects of phytoconstituents on various biomarkers associated with various cancer types.
| S.No. | Phytoconstituent | Type of cancer | Biomarkers | Application of biomarker | Outcome | Reference |
|---|---|---|---|---|---|---|
| 1. | Resveratrol | Colorectal | Ki-67 | Cancer proliferation | It leads to downregulation of Ki-67 levels on the growth and progression of malignancy. | Patel et al. (160) |
| Caspase-3 | Apoptosis | It led to an increase in cleaved caspase-3 levels within malignant hepatic tissue. | Howells et al. (161) | |||
| Breast | RASSF1α | Detection and prognosis | The reduction of methylation levels in the RASSF-1α gene on administration of resveratrol. | Zhu et al. (162) | ||
| Prostate | Ki-67 | Cancer proliferation | Significant reduction in the levels of cellular proliferation markers, specifically Ki67. | Singh et al. (163) | ||
| PCNA | Cancer proliferation | Reduction in the levels of PCNA, a well-established marker of cell survival, has been observed upon exposure to resveratrol. | Singh et al. (163) | |||
| 2. | Curcumin | Breast | miRNA-203 | Diagnosis | It leads to an increase in miR-203 which shows promising therapy against cancer by regulating epigenetic code, a key mechanism involved in the development and progression of breast cancer. | Khan et al. (164) |
| Bladder | Ki-67 | Cancer proliferation | The findings of this study demonstrate a notable reduction in Ki-67 expression. | Kamat et al. (165) | ||
| Prostate | PCNA | Cancer proliferation | Significant reduction in PCNA levels, which subsequently leads to the activation of apoptosis of malignant cells. | Barve et al. (166) | ||
| Pancreatic | miRNA-22 | Diagnostic | The up-regulation of miRNA-22, induced by curcumin, has been found to exhibit inhibitory effects on the growth of pancreatic cancer cells. | Khan et al. (164) | ||
| Hepatic | miRNA-21 | Diagnosis | The decline in miR-21 has been found to play a crucial role in facilitating the regulation of the cell cycle and apoptosis by elevating PTEN and PDCD4 Protein level in Hepatic cancer. | Khan et al. (164) | ||
| 3. | Quercetin | Breast | EZH2 | Prognostic | The inhibition of EZH2 has been found to have a substantial impact by effectively blocking the Notch-1 and P13K/Akt signal pathways. | Cao et al. (167) |
| Liver | AFP | Diagnosis | The intervention demonstrated significant efficacy in reducing the incidence of AFP rates. | Abdu et al. (168) | ||
| Prostate | Hsp90 | Diagnosis | The stimulation of cell death and caspases through the inhibition of Hsp90 was observed. | Aalinkeel et al. (169) | ||
| Thyroid | Pro-NAG1 | Diagnosis | The induction of apoptosis was observed to be mediated through the selective upregulation of pro-NAG-1 expression. | Hong et al. (170) | ||
| 4. | Beta lapachone | Breast | NQO1 | Prognosis | The inhibitory effects of β-lapachone on the Akt/mTOR signaling pathway were observed through the downregulation of NQO1. | Yang et al. (171) |
| Pancreatic | NQO1 | Prognosis | The administration of β-lapachone resulted in a significant reduction in NQO-1 levels. | Silvers et al. (172) | ||
| 5. | Epigallocatechin | Breast | Akt | Indication of regulation of P13K/mTOR pathway | The inhibitory effects of polyphenol treatment on AKT were observed at both the RNA and protein levels resulting in cancer’s attenuation. | Thangapazham et al. (173) |
| p53 | Diagnosis | It inhibits the development of malignant breast cells and induces apoptosis through deregulating the P53/Bcl-2 pathway. | Huang et al (174) | |||
| Hepatic | Ki-67 and PCNA | Cell proliferation | A significant decrease in the expression levels of PCNA and Ki-67 which results in inhibitory effects on cellular proliferation in the liver. | Sojoodi et al. (175) | ||
| Bladder | PCNA | Cell proliferation | A significant decrease in the biomarker levels, which was found to be dependent on the dosage administered. | Piwowarczyk et al. (176) | ||
| IL-1β | Inflammation | IL-1β suppression decreases formation of ROS, AP-1/NF-kB, and cancer cell migration. | Sah et al. (177) | |||
| Colon | ACF | Prognosis | The formation of ACF was found to be markedly suppressed, as evidenced by a notable reduction in their size within cancer cells. | Zhong et al. (178) | ||
| 6. | Ellagic acid | Breast | Actinin-4 (ACTN4) | Early diagnosis and prediction | The inhibitory effects on ACTN4 led to the suppression of cancerous cell multiplication and colony formation by declining β-catenin proteasome. | Wang et al. (84, 85) |
| Hepatic | AFP | Diagnosis | There was a substantial reduction in the concentration of AFP. | Zaazaa et al. (179) | ||
| Oral | Birc5 | Diagnosis and prognosis | It effectively impedes tumor cell proliferation and hinder disease progression by diminishing anti-apoptotic associated Birc5 marker. | Oghumu et al. (180) | ||
| 7. | Daidzein | Breast | Caspase-9 | Apoptosis | Increase in caspase-9 activity by 32.2% upon exposure to Daidzein, leading to the induction of apoptosis. | Choi et al. (181) |
| 8. | Dihydroartemisinin | Brain | HSPA-5 | ER stress | HSPA5, a key marker of ER stress was increased which inhibits the PERK/ATF4 pathway. | Chen et al. (182) |
| Colon | c-MYC | Diagnosis | A decrease in the levels of the c-MYC protein, a pivotal modulator of several cellular processes, through the proteasome pathway. | Lu et al. (183) | ||
| Hepatic | ANGPTL 2 | Cellular Senescence | The inhibition of multiplication and invasion in glioma cells has been attributed to the decline in ANGPTL2 levels, which effectively suppresses the ERK/MAPK pathway. | Wu et al. (184) | ||
| Ovarian | PDGFRα | Prognostic | The interruption of PDGFRα by DHA results in interruption of cell growth, multiplication, and apoptosis in malignant cells. | Li et al. (185) | ||
| 9. | Triptolide | Adeno (Stomach) | CXCR4 | Prognostic | The therapeutic targeting of CXCR4 by triptolide holds significant promise in the realm of cancer treatment. | Qiu et al. (186) |
| Pancreatic | KRAS | Diagnosis | A significant reduction in KRAS mutation levels in cancer cells, leading to a notable antitumor effect. | Kim et al. (187) | ||
| 10. | Genistein | Breast | miR-23b | Inflammation | It upregulates miR-23b effectively inhibits cell migration and metastasis. | Avci et al. (188) |
| Colon | TTTY18 | Cancer development/metastasis | A significant reduction in tumor volume, accompanied by decrease in both TGF-β1 contents and TTTY18. | Chen et al. (189) | ||
| Ovarian | Malondialdehyde | Oxidative stress | The intervention resulted in a decrease in the marker and level of NFkB, while simultaneously increasing Nrf2 and Bax in cancer cells. | Sahin et al. (190) |