Inhibition of MKK7-JNK by the TOR signaling pathway regulator-like protein contributes to resistance of HCC cells to TRAIL-induced apoptosis

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dc.contributor.authorIn Sung Song-
dc.contributor.authorSoo Young Jun-
dc.contributor.authorH J Na-
dc.contributor.authorH T Kim-
dc.contributor.authorS Y Jung-
dc.contributor.authorG H Ha-
dc.contributor.authorYoung-Ho Park-
dc.contributor.authorL Z Long-
dc.contributor.authorDae Yeul Yu-
dc.contributor.authorJ M Kim-
dc.contributor.authorJ H Kim-
dc.contributor.authorJeong Heon Ko-
dc.contributor.authorC H Kim-
dc.contributor.authorNam-Soon Kim-
dc.date.accessioned2017-04-19T09:35:31Z-
dc.date.available2017-04-19T09:35:31Z-
dc.date.issued2012-
dc.identifier.issn0016-5085-
dc.identifier.uri10.1053/j.gastro.2012.07.103ko
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/11038-
dc.description.abstractBackground & Aims: The TOR signaling pathway regulator-like (TIPRL) protein, the mammalian ortholog of yeast TIP41, was identified in an expression profiling screen for factors that regulate human liver carcinogenesis. We investigated the role of human TIPRL protein in hepatocellular carcinoma (HCC). Methods: We measured the level of TIPRL in HCC and adjacent nontumor tissues from patients. We used small interfering RNAs and zebrafish to study the function of TIPRL. We used annexin V propidium iodide staining and immunoblot analyses to measure apoptosis and activation of apoptotic signaling pathways. We used confocal microscopy, coimmunoprecipitation, and glutathione-S transferase pull-down analyses to determine interactions among mitogen-activated protein kinase kinase 7 (MKK7 or MAP2K7), TIPRL, and the protein phosphatase type 2A (PP2Ac). We studied the effects of TIPRL in tumor xenografts in mice. Results: Levels of TIPRL were higher in HCC tissues and cell lines than nontumor tissues and primary hepatocytes. Knockdown of tiprl expression in zebrafish led to large amounts of apoptosis throughout the embryos. Incubation of HCC cells, but not primary human hepatocytes, with small interfering RNA against TIPRL (siTIPRL) and tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) caused prolonged activation (phosphorylation) of MKK7 and c-Jun N-terminal kinase (JNK) and led to apoptosis, indicated by cleavage of procaspase-8,-3 and of poly-(adenosine diphosphate-ribose) polymerase. TIPRL bound to MKK7 and PP2Ac and promoted the interaction between MKK7 and PP2Ac. In mice, injection of HCC xenograft tumors with siTIPRL and TRAIL led to tumor apoptosis and regression. Conclusions: TIPRL is highly up-regulated in human HCC samples and cell lines, compared with noncancerous liver tissues. TIPRL prevents prolonged activation of MKK7 and JNK and TRAIL-induced apoptosis by mediating the interaction between MKK7 and PP2Ac.-
dc.publisherElsevier-
dc.titleInhibition of MKK7-JNK by the TOR signaling pathway regulator-like protein contributes to resistance of HCC cells to TRAIL-induced apoptosis-
dc.title.alternativeInhibition of MKK7-JNK by the TOR signaling pathway regulator-like protein contributes to resistance of HCC cells to TRAIL-induced apoptosis-
dc.typeArticle-
dc.citation.titleGastroenterology-
dc.citation.number5-
dc.citation.endPage1351-
dc.citation.startPage1341-
dc.citation.volume143-
dc.contributor.affiliatedAuthorIn Sung Song-
dc.contributor.affiliatedAuthorSoo Young Jun-
dc.contributor.affiliatedAuthorYoung-Ho Park-
dc.contributor.affiliatedAuthorDae Yeul Yu-
dc.contributor.affiliatedAuthorJeong Heon Ko-
dc.contributor.affiliatedAuthorNam-Soon Kim-
dc.contributor.alternativeName송인성-
dc.contributor.alternativeName전수영-
dc.contributor.alternativeName나희준-
dc.contributor.alternativeName김현택-
dc.contributor.alternativeName정소영-
dc.contributor.alternativeName하가희-
dc.contributor.alternativeName박영호-
dc.contributor.alternativeNameLong-
dc.contributor.alternativeName유대열-
dc.contributor.alternativeName김진만-
dc.contributor.alternativeName김주헌-
dc.contributor.alternativeName고정헌-
dc.contributor.alternativeName김철희-
dc.contributor.alternativeName김남순-
dc.identifier.bibliographicCitationGastroenterology, vol. 143, no. 5, pp. 1341-1351-
dc.identifier.doi10.1053/j.gastro.2012.07.103-
dc.subject.keywordChemotherapy Resistance Mechanisms-
dc.subject.keywordLiver Cancer-
dc.subject.keywordTumor Cell Death-
dc.subject.localChemotherapy Resistance Mechanisms-
dc.subject.localLiver cancer-
dc.subject.localliver cancer-
dc.subject.localLiver Cancer-
dc.subject.localTumor Cell Death-
dc.description.journalClassY-
Appears in Collections:
Ochang Branch Institute > Division of National Bio-Infrastructure > Futuristic Animal Resource & Research Center > 1. Journal Articles
Synthetic Biology and Bioengineering Research Institute > Genome Editing Research Center > 1. Journal Articles
Division of Biomedical Research > Rare Disease Research Center > 1. Journal Articles
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