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Long non-coding RNA MEG3 functions as a tumour suppressor and has prognostic predictive value in human pancreatic cancer.
Ma, Ling; Wang, Feng; Du, Chong; Zhang, Zhengkui; Guo, Huahu; Xie, Xuehai; Gao, Hongqiao; Zhuang, Yan; Kornmann, Marko; Gao, Hong; Tian, Xiaodong; Yang, Yinmo.
Afiliação
  • Ma L; Department of General Surgery, Peking University First Hospital, Beijing 100034, P.R. China.
  • Wang F; Department of General Surgery, Peking University First Hospital, Beijing 100034, P.R. China.
  • Du C; Department of General Surgery, Peking University First Hospital, Beijing 100034, P.R. China.
  • Zhang Z; Department of General Surgery, Peking University First Hospital, Beijing 100034, P.R. China.
  • Guo H; Department of General Surgery, Peking University First Hospital, Beijing 100034, P.R. China.
  • Xie X; Department of General Surgery, Peking University First Hospital, Beijing 100034, P.R. China.
  • Gao H; Department of General Surgery, Peking University First Hospital, Beijing 100034, P.R. China.
  • Zhuang Y; Department of General Surgery, Peking University First Hospital, Beijing 100034, P.R. China.
  • Kornmann M; Clinic of General, Visceral and Transplantation Surgery, University of Ulm, D-89081 Ulm, Germany.
  • Gao H; Department of Surgical Oncology, Peking University Ninth School of Clinical Medicine (Beijing Shijitan Hospital, Capital Medical University), Beijing 100038, P.R. China.
  • Tian X; Department of General Surgery, Peking University First Hospital, Beijing 100034, P.R. China.
  • Yang Y; Department of General Surgery, Peking University First Hospital, Beijing 100034, P.R. China.
Oncol Rep ; 39(3): 1132-1140, 2018 Mar.
Article em En | MEDLINE | ID: mdl-29328401
Long non-coding RNA (lncRNA) MEG3 has been demonstrated to be a tumour suppressor in many malignancies. However, the functional role of MEG3 in pancreatic cancer (PC) is unclear. In this study, the expression pattern of MEG3 was evaluated in 25 samples of microdissected PC tissues and 8 PC cell lines and was compared to the expression in adjacent non­cancerous tissues and a human pancreatic normal epithelial cell line. Loss of MEG3 expression was observed in both the cancerous tissues and cancer cell lines. Although the absence of expression of MEG3 was not statistically correlated to either histological grade or TNM stage in the 25 cases, the prognosis was significantly worse. MEG3 knockdown enhanced cell proliferation, promoted cell migration and invasion, induced epithelial­mesenchymal transition (EMT), increased the sphere­forming ability and cancer stem cell (CSC) properties, and decreased the chemosensitivity to gemcitabine in vitro. In contrast, forced expression of MEG3 resulted in a reverse effect. In conclusion, MEG3 functions as a tumour suppressor in human PC. The underlying cause of the poor prognosis induced by low levels of MEG3 expression in PC patients might involve EMT induction, enhanced CSC phenotypes and reduced chemoresistance, all of which might be associated with Snail activation.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Pancreáticas / Biomarcadores Tumorais / Regulação Neoplásica da Expressão Gênica / Resistencia a Medicamentos Antineoplásicos / Transição Epitelial-Mesenquimal / RNA Longo não Codificante Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Pancreáticas / Biomarcadores Tumorais / Regulação Neoplásica da Expressão Gênica / Resistencia a Medicamentos Antineoplásicos / Transição Epitelial-Mesenquimal / RNA Longo não Codificante Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male Idioma: En Ano de publicação: 2018 Tipo de documento: Article