Qin Chengwei, Zhao Yanming, Gong Chunzhi, Yang Zhenlin
Department of General Surgery, Medical College of Shandong University, Jinan, Shandong 250012, P.R. China.
Department of Anesthesiology, Binzhou Medical University Hospital, Binzhou, Shandong 256603, P.R. China.
Oncol Lett. 2017 Dec;14(6):6969-6975. doi: 10.3892/ol.2017.7021. Epub 2017 Sep 21.
Breast cancer is the leading cause for cancer-associated mortality in women. Although great progress has been made in the earlier diagnosis and systemic therapy of patients with breast cancer in recent years, recurrence or distant metastasis continue to present major barriers to the successful treatment of breast cancer. Therefore, fully understanding the molecular mechanisms underlying the progression of breast cancer may be critical for the development of effective therapeutic strategies against breast cancer. The aim of the present study was to explore the expression, function and molecular mechanisms of microRNA-154 (miR-154) in human breast cancer. It was demonstrated that miR-154 was significantly downregulated in breast cancer tissue and cell lines. The restoration of miR-154 expression suppressed the proliferation, migration and invasion of breast cancer cells. ADAM metallopeptidase domain 9 (ADAM9) was identified as a novel direct target for miR-154 in breast cancer. It was demonstrated that miR-154 acted as a tumor suppressor in breast cancer by targeting ADAM9. The results of the present study suggest that the restoration of miR-154 expression may be an effective therapeutic strategy for the treatment of breast cancer in the future.
乳腺癌是女性癌症相关死亡的主要原因。尽管近年来乳腺癌患者的早期诊断和全身治疗取得了巨大进展,但复发或远处转移仍然是乳腺癌成功治疗的主要障碍。因此,充分了解乳腺癌进展的分子机制对于开发有效的乳腺癌治疗策略可能至关重要。本研究的目的是探讨微小RNA-154(miR-154)在人类乳腺癌中的表达、功能及分子机制。结果表明,miR-154在乳腺癌组织和细胞系中显著下调。miR-154表达的恢复抑制了乳腺癌细胞的增殖、迁移和侵袭。金属蛋白酶解整合素结构域9(ADAM9)被确定为乳腺癌中miR-154的一个新的直接靶点。结果表明,miR-154通过靶向ADAM9在乳腺癌中发挥肿瘤抑制作用。本研究结果表明,恢复miR-154表达可能是未来治疗乳腺癌的一种有效治疗策略。