Department of Surgery, University of Maryland School of Medicine, Baltimore, Maryland, United States of America.
Department of Medicine, Division of Gastroenterology & Hepatology, University of Maryland School of Medicine, Baltimore, Maryland, United States of America.
PLoS One. 2022 Jun 3;17(6):e0269618. doi: 10.1371/journal.pone.0269618. eCollection 2022.
Overexpression of M3 subtype muscarinic receptors (M3R) hastens colon cancer progression. As microRNA (miRNA) expression is commonly dysregulated in cancer, we used microarrays to examine miRNA profiles in muscarinic receptor agonist-treated human colon cancer cells. We used quantitative RT-PCR (qPCR) to validate microarray results and examine miRNA expression in colon cancers and adjacent normal colon. These assays revealed that acetylcholine (ACh) treatment robustly induced miR-222 expression; miR-222 levels were three-fold higher in cancer compared to normal colon. In kinetic studies, ACh induced a 4.6-fold increase in pri-miR-222 levels within 1 h, while mature miR-222 increased gradually to 1.8-fold within 4 h. To identify post-M3R signaling mediating these actions, we used chemical inhibitors and agonists. ACh-induced increases in pri-miR-222 were attenuated by pre-incubating cells with atropine and inhibitors of protein kinase C (PKC) and p38 MAPK. Treatment with a PKC agonist, phorbol 12-myristate 13-acetate, increased pri-miR-222 levels, an effect blocked by PKC and p38 MAPK inhibitors, but not by atropine. Notably, treatment with ACh or transfection with miR-222 mimics increased cell proliferation; atropine blocked the effects of ACh but not miR-222. These findings identify a novel mechanism whereby post-M3R PKC/p38 MAPK signaling stimulates miR-222 expression and colon cancer cell proliferation.
M3 亚型毒蕈碱受体 (M3R) 的过表达会加速结肠癌的进展。由于 miRNA (miRNA) 在癌症中通常存在表达失调,我们使用微阵列来检查毒蕈碱受体激动剂处理的人结肠癌细胞中的 miRNA 谱。我们使用定量 RT-PCR (qPCR) 来验证微阵列结果,并检查结肠癌和相邻正常结肠中的 miRNA 表达。这些检测显示,乙酰胆碱 (ACh) 处理可强烈诱导 miR-222 的表达;与正常结肠相比,癌症中的 miR-222 水平高出三倍。在动力学研究中,ACh 在 1 小时内诱导 pri-miR-222 水平增加了 4.6 倍,而成熟的 miR-222 逐渐增加到 4 小时内的 1.8 倍。为了确定介导这些作用的 M3R 后信号,我们使用了化学抑制剂和激动剂。在用阿托品和蛋白激酶 C (PKC) 和 p38 MAPK 的抑制剂预先孵育细胞后,ACh 诱导的 pri-miR-222 增加被减弱。用 PKC 激动剂佛波醇 12-肉豆蔻酸 13-醋酸盐处理可增加 pri-miR-222 水平,该作用被 PKC 和 p38 MAPK 抑制剂阻断,但不被阿托品阻断。值得注意的是,用 ACh 处理或转染 miR-222 模拟物可增加细胞增殖;阿托品阻断了 ACh 的作用,但不阻断 miR-222 的作用。这些发现确定了一种新的机制,即 M3R 后 PKC/p38 MAPK 信号刺激 miR-222 表达和结肠癌细胞增殖。