The long non-coding RNA HOTTIP promotes progression and gemcitabine resistance by regulating HOXA13 in pancreatic cancerReportar como inadecuado

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Journal of Translational Medicine

, 13:84

First Online: 12 March 2015Received: 21 October 2014Accepted: 18 February 2015DOI: 10.1186-s12967-015-0442-z

Cite this article as: Li, Z., Zhao, X., Zhou, Y. et al. J Transl Med 2015 13: 84. doi:10.1186-s12967-015-0442-z


BackgroundThe human genome encodes many long non-coding RNAs lncRNAs. However, their biological functions, molecular mechanisms, and the prognostic value associated with pancreatic ductal adenocarcinoma PDAC remain to be elucidated. Here, we identify a fundamental role for the lncRNA HOXA transcript at the distal tip HOTTIP in the progression and chemoresistance of PDAC.

MethodsHigh-throughput microarrays were performed to detect the expression profiles of lncRNAs and messenger RNAs in eight human PDAC tissues and four pancreatic tissues. Quantitative real-time PCR was used to determine the levels of HOTTIP and HOXA13 transcripts in PDAC cell lines and 90 PDAC samples from patients. HPDE6 cells immortalized human pancreatic ductal epithelial cells and corresponding adjacent non-neoplastic tissues were used as controls, respectively. The functions of HOTTIP and HOXA13 in cell proliferation, invasion, and epithelial-mesenchymal transition were evaluated by targeted knockdown in vitro. CCK-8 assays, colony formation assays, and xenografts in nude mice were used to investigate whether targeted silencing of HOTTIP could sensitize pancreatic cancer cells to gemcitabine. Immunohistochemistry was performed to investigate the relationship between HOXA13 expression and patient outcome.

ResultsMicroarray analyses revealed that HOTTIP was one of the most significantly upregulated lncRNAs in PDAC tissues compared with pancreatic tissues. Quantitative PCR further verified that HOTTIP levels were increased in PDAC cell lines and patient samples compared with controls. Functionally, HOTTIP silencing resulted in proliferation arrest by altering cell-cycle progression, and impaired cell invasion by inhibiting epithelial-mesenchymal transition in pancreatic cancer. Additionally, inhibition of HOTTIP potentiated the antitumor effects of gemcitabine in vitro and in vivo. Furthermore, knockdown of HOXA13 by RNA interference siHOXA13 revealed that HOTTIP promoted PDAC cell proliferation, invasion, and chemoresistance, at least partly through regulating HOXA13. Immunohistochemistry results revealed that higher HOXA13 expression was correlated with lymph node metastasis, poor histological differentiation, and decreased overall survival in PDAC patients.

ConclusionsAs a crucial tumor promoter, HOTTIP promotes cell proliferation, invasion, and chemoresistance by modulating HOXA13. Therefore, the HOTTIP-HOXA13 axis is a potential therapeutic target and molecular biomarker for PDAC.

KeywordsPancreatic cancer HOTTIP Oncogenic Epithelial-mesenchymal transition Chemoresistance AbbreviationsPCPancreatic cancer

PDACPancreatic ductal adenocarcinoma

HOTTIPHOXA transcript at the distal tip

EMTEpithelial mesenchymal transition

lncRNALong non-coding RNA

Zhihua Li and Xiaohui Zhao contributed equally to this work.

Electronic supplementary materialThe online version of this article doi:10.1186-s12967-015-0442-z contains supplementary material, which is available to authorized users.

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Autor: Zhihua Li - Xiaohui Zhao - Yu Zhou - Yimin Liu - Quanbo Zhou - Huilin Ye - YinXue Wang - Jinlong Zeng - Yadong Song - Wen


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