Decyl caffeic acid inhibits the proliferation of colorectal cancer cells in an autophagy-dependent manner in vitro and in vivo

• Published in: PloS one 2020-05, Vol.15 (5), p.e0232832-e0232832
• Main Authors: Chen, Ching, Kuo, Yueh-Hsiung, Lin, Cheng-Chieh, Chao, Che-Yi, Pai, Man-Hui, Chiang, En-Pei Isabel, Tang, Feng-Yao
• Format: Article
• Language: English
• Subjects: Acids; Adenocarcinoma; AKT protein; Animal models; Anticancer properties; Apoptosis; Autophagy; Autophagy (Cytology); Biology and Life Sciences; Biotechnology; Caffeic acid; Cancer cells; Cancer therapies; Cancer treatment; Care and treatment; Cascades; Cell cycle; Cell death; Cell growth; Cell proliferation; Cell survival; Chemical compounds; Chemotherapy; Colorectal cancer; Colorectal carcinoma; Cyclin A; Cyclin E; Development and progression; Esters; Flow cytometry; Health aspects; In vivo methods and tests; Kinases; Laboratories; Medicine; Medicine and Health Sciences; Molecular modelling; Novels; Nutrition; Phagocytosis; Pharmacology; Phosphorylation; Physiological aspects; Proteins; Regulators; Research and analysis methods; S phase; Signaling; Stat3 protein; Studies; Surgical implants; Survival; Tumors; Xenografts; Xenotransplantation
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0232832

The treatment of human colorectal cancer (CRC) cells through suppressing the abnormal survival signaling pathways has recently become a significant area of focus. In this study, our results demonstrated that decyl caffeic acid (DC), one of the novel caffeic acid derivatives, remarkedly suppressed the growth of CRC cells both in vitro and in vivo. The inhibitory effects of DC on CRC cells were investigated in an in vitro cell model and in vivo using a xenograft mouse model. CRC cells were treated with DC at various dosages (0, 10, 20 and 40 μM), and cell survival, the apoptotic index and the autophagy level were measured using an MTT assay and flow cytometry analysis, respectively. The signaling cascades in CRC were examined by Western blot assay. The anti-cancer effects of DC on tumor growth were examined by using CRC HCT-116 cells implanted in an animal model. Our results indicated that DC differentially suppressed the growth of CRC HT-29 and HCT-116 cells through an enhancement of cell-cycle arrest at the S phase. DC inhibited the expression of cell-cycle regulators, which include cyclin E and cyclin A proteins. The molecular mechanisms of action were correlated to the blockade of the STAT3 and Akt signaling cascades. Strikingly, a high dosage of DC prompted a self-protection action through inducing cell-dependent autophagy in HCT-116 cells. Suppression of autophagy induced cell death in the treatment of DC in HCT-116 cells. DC seemed to inhibit cell proliferation of CRC differentially, and the therapeutic advantage appeared to be autophagy dependent. Moreover, consumption of DC blocked the tumor growth of colorectal adenocarcinoma in an experimental animal model. In conclusion, our results suggested that DC could act as a therapeutic agent through the significant suppression of tumor growth of human CRC cells.