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Reciprocal activation between STAT3 and miR-181b regulates the proliferation of esophageal cancer stem-like cells via the CYLD pathway.
Xu, Dan-Dan; Zhou, Peng-Jun; Wang, Ying; Zhang, Li; Fu, Wu-Yu; Ruan, Bi-Bo; Xu, Hai-Peng; Hu, Chao-Zhi; Tian, Lu; Qin, Jin-Hong; Wang, Sheng; Wang, Xiao; Li, Yi-Cheng; Liu, Qiu-Ying; Ren, Zhe; Zhang, Rong; Wang, Yi-Fei.
Afiliação
  • Xu DD; College of Life Science and Technology, Jinan University, 510632, Guangzhou, P.R. China.
  • Zhou PJ; Key laboratory of Bioengineering medicine of Guangdong Province, Jinan University, 510632, Guangzhou, P.R. China.
  • Wang Y; Department of Pathogen Biology and Immunology, School of Basic Course, Guangdong Pharmaceutical University, Guangzhou, 510006, P.R. China.
  • Zhang L; College of Life Science and Technology, Jinan University, 510632, Guangzhou, P.R. China.
  • Fu WY; Faculty of Environmental and Biological Engineering, Guangdong University of Petrochemical Technology, 525000, Maoming, P.R. China.
  • Ruan BB; College of Life Science and Technology, Jinan University, 510632, Guangzhou, P.R. China.
  • Xu HP; School of Traditional Chinese Medicine, Guangdong Pharmaceutical University, Guangzhou, 510006, P.R. China.
  • Hu CZ; School of Traditional Chinese Medicine, Guangdong Pharmaceutical University, Guangzhou, 510006, P.R. China.
  • Tian L; College of Life Science and Technology, Jinan University, 510632, Guangzhou, P.R. China.
  • Qin JH; College of Life Science and Technology, Jinan University, 510632, Guangzhou, P.R. China.
  • Wang S; College of Life Science and Technology, Jinan University, 510632, Guangzhou, P.R. China.
  • Wang X; College of Life Science and Technology, Jinan University, 510632, Guangzhou, P.R. China.
  • Li YC; College of Life Science and Technology, Jinan University, 510632, Guangzhou, P.R. China.
  • Liu QY; College of Life Science and Technology, Jinan University, 510632, Guangzhou, P.R. China.
  • Ren Z; College of Life Science and Technology, Jinan University, 510632, Guangzhou, P.R. China.
  • Zhang R; College of Life Science and Technology, Jinan University, 510632, Guangzhou, P.R. China.
  • Wang YF; College of Life Science and Technology, Jinan University, 510632, Guangzhou, P.R. China.
Mol Cancer ; 15(1): 40, 2016 05 17.
Article em En | MEDLINE | ID: mdl-27189061
ABSTRACT

BACKGROUND:

Recent studies have suggested that cancer cells contain subpopulations that can initiate tumor growth, self-renew, and maintain tumor cell growth. However, for esophageal cancer cells, the relationship between STAT3, microRNAs and cancer stem cells remains unclear.

METHODS:

Serum-free culture was used to enrich esophageal cancer stem-like cells (ECSLC). Flow cytometry determined the proportion of ECSLC. qPCR were performed to examine expression level of stemness factors, mesenchymal markers, ATP-binding cassette (ABC) transporters, STAT3, miR-181b, CYLD. Western blot were performed to analyze the expression of STAT3, p-STAT3 and CYLD (cylindromatosis). BALB/c mice xenograft studies were conducted to evaluate the tumorigenicity of enriched ECSLC. Sphere formation assay and colony formation assays were employed to analyze the relationship between STAT3 and miR-181b. Luciferase assays were used to evaluate activity which CYLD is a target of miR-181b.

RESULTS:

Sphere formation cells (SFCs) with properties of ECSLC were enriched. Enriched SFCs in serum-free suspension culture exhibited cancer stem-like cell properties and increased single-positive CD44 + CD24-, stemness factor, mesenchymal marker expression ABC transporters and tumorigenicity in vivo compared with the parental cells. Additionally, we found that reciprocal activation between STAT3 and miR-181b regulated SFCs proliferation. Moreover, STAT3 directly activated miR-181b transcription in SFCs and miR-181b then potentiated p-STAT3 activity. Luciferase assays indicated that CYLD was a direct and functional target of miR-181b.

CONCLUSION:

The mutual regulation between STAT3 and miR-181b in SFCs was required for proliferation and apoptosis resistance. STAT3 and miR-181b control each other's expression in a positive feedback loop that regulates SFCs via CYLD pathway. These findings maybe is helpful for targeting ECSLC and providing approach for esophageal cancer treatments.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Células-Tronco Neoplásicas / Neoplasias Esofágicas / Transdução de Sinais / Proteínas Supressoras de Tumor / MicroRNAs / Fator de Transcrição STAT3 Tipo de estudo: Prognostic_studies Limite: Animals / Humans Idioma: En Revista: Mol Cancer Assunto da revista: NEOPLASIAS Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Células-Tronco Neoplásicas / Neoplasias Esofágicas / Transdução de Sinais / Proteínas Supressoras de Tumor / MicroRNAs / Fator de Transcrição STAT3 Tipo de estudo: Prognostic_studies Limite: Animals / Humans Idioma: En Revista: Mol Cancer Assunto da revista: NEOPLASIAS Ano de publicação: 2016 Tipo de documento: Article