The contrary functions of lnc RNA HOTAIR /miR‐17‐5p/ PTEN axis and Shenqifuzheng injection on chemosensitivity of gastric cancer cells

This study was implemented to figure out whether lnc RNA HOTAIR /miR‐17‐5p/ PTEN axis played a role that was opposite to Shenqifuzheng ( SQFZ ) injection in regulating the chemosensitivity of gastric cancer cells. The gastric cancer tissues were gathered and four gastric cancer cell lines were prepa...

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Published inJournal of cellular and molecular medicine Vol. 23; no. 1; pp. 656 - 669
Main Authors Jia, Jianguang, Zhan, Dankai, Li, Jing, Li, Zhixiang, Li, Hongbo, Qian, Jun
Format Journal Article
LanguageEnglish
Published Chichester John Wiley & Sons, Inc 01.01.2019
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ISSN1582-1838
1582-4934
DOI10.1111/jcmm.13970

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Summary:This study was implemented to figure out whether lnc RNA HOTAIR /miR‐17‐5p/ PTEN axis played a role that was opposite to Shenqifuzheng ( SQFZ ) injection in regulating the chemosensitivity of gastric cancer cells. The gastric cancer tissues were gathered and four gastric cancer cell lines were prepared, including BGC ‐823, MGC ‐803, SGC ‐7901, and MKN 28. Moreover, cisplatin, adriamycin, mitomycin, and 5‐fluoroura were managed as the chemo‐therapeutics, and SQFZ was prepared as a Chinese medicine. Striking distinctions of HOTAIR , miR‐17‐5p, and PTEN expressions were observed between gastric cancer tissues and para‐carcinoma normal tissues ( P  <   0.05). MKN 28 was associated with the highest resistance to cisplatin, adriamycin, mitomycin, and 5‐fluoroura among all the cell types, and SQFZ significantly improved the MKN 28 cells’ sensitivity to the drugs ( P  <   0.05). The over‐expressed HOTAIR and miR‐17‐5p, as well as under‐expressed PTEN tended to significantly facilitate the viability, EMT process and proliferation of MKN 28 cells that were subject to treatment of chemo‐therapies ( P  <   0.05). SQFZ could amplify the effects of si‐ HOTAIR , miR‐17‐5p inhibitor, and pc DNA ‐ PTEN on boosting the chemosensitivity of gastric cancer cells ( P  <   0.05). In addition, HOTAIR was also found to directly target miR‐17‐5p, and PTEN appeared to be subject to the modification of HOTAIR and miR‐17‐5p in its acting on the viability, proliferation, EMT process, and apoptosis of gastric cancer cells. The HOTAIR /miR‐17‐5p/ PTEN axis could be regarded as the potential treatment targets for gastric cancer, and adjuvant therapy of SQFZ injection could assist in further improving the treatment efficacy of chemo‐therapies for gastric cancer.
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ISSN:1582-1838
1582-4934
DOI:10.1111/jcmm.13970