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MiR-200b regulates autophagy associated with chemoresistance in human lung adenocarcinoma
Author(s) -
Banzhou Pan,
Bing Feng,
Yitian Chen,
Guichun Huang,
Rui Wang,
Longbang Chen,
Haizhu Song
Publication year - 2015
Publication title -
oncotarget
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.373
H-Index - 127
ISSN - 1949-2553
DOI - 10.18632/oncotarget.5352
Subject(s) - atg12 , downregulation and upregulation , autophagy , cancer research , medicine , microrna , adenocarcinoma , in vivo , apoptosis , oncology , biology , cancer , gene , atg5 , biochemistry , microbiology and biotechnology
Chemoresistance remains a major clinical problem in combating human lung adenocarcinoma (LAD), and abnormal autophagy is closely associated with this phenomenon. In the present study, an inverse correlation between miR-200b and autophagy-associated gene 12 (ATG12) expressions was observed in docetaxel-resistant (SPC-A1/DTX and H1299/DTX) and sensitive (SPC-A1 and H1299) LAD cells as well as in tissue samples. Further study showed that miR-200b directly targeted ATG12 in LAD. Moreover, miR-200b-dependent ATG12 downregulation inhibited autophagy and enhanced the chemosensitivity of SPC-A1/DTX and H1299/DTX cells both in vivo and in vitro. LAD chemoresistance is therefore closely related to downregulation of miR-200b and the corresponding upregulation of ATG12. These results provide new evidence for the mechanisms governing the microRNA (miRNA)-ATG12 network and their possible contribution to autophagy modulation and LAD chemoresistance.

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