Stem Cell Research Center, Korea Research Institute of Bioscience and Biotechnology, Daejeon 34141, Republic of Korea.
Mol Med Rep. 2019 Aug;20(2):1569-1574. doi: 10.3892/mmr.2019.10431. Epub 2019 Jun 26.
Short‑chain fatty acids (SCFAs; butyrate, propionate and acetate) are metabolites derived from the gut microbiota via dietary fiber fermentation. In colon cancer, treatment with SCFAs, mainly butyrate and propionate, suppresses cell proliferation, migration and invasion. Furthermore, although sodium butyrate is known to induce cell apoptosis in lung cancer, the anticancer effects of sodium propionate (SP) on lung cancer are not well understood. In the present study, SP treatment induced cell cycle arrest, especially in the G2/M phase, and cell apoptosis in the H1299 and H1703 lung cancer cell lines. As determined by reverse transcription‑quantitative PCR and western blotting, Survivin and p21 expression levels were significantly affected by SP treatment, suggesting that SP treatment suppressed cell proliferation in these lung cancer cell lines. Thus, it was proposed that the SP‑mediated regulation of Survivin and p21 in lung cancer may be applicable to lung cancer therapy.
短链脂肪酸(SCFAs;丁酸盐、丙酸盐和醋酸盐)是膳食纤维发酵产生的肠道微生物群的代谢产物。在结肠癌中,SCFAs(主要是丁酸盐和丙酸盐)的治疗可抑制细胞增殖、迁移和侵袭。此外,虽然丁酸钠已知可诱导肺癌细胞凋亡,但丙酸钠(SP)对肺癌的抗癌作用尚不清楚。在本研究中,SP 处理诱导细胞周期停滞,特别是在 G2/M 期,以及 H1299 和 H1703 肺癌细胞系中的细胞凋亡。通过逆转录-定量 PCR 和 Western blot 测定,Survivin 和 p21 的表达水平受 SP 处理的显著影响,表明 SP 处理抑制了这些肺癌细胞系中的细胞增殖。因此,有人提出,SP 介导的肺癌中 Survivin 和 p21 的调节可能适用于肺癌治疗。