Transglutaminase 2 inhibition found to induce p53 mediated apoptosis in renal cell carcinoma

被引:48
作者
Ku, Bo Mi [1 ]
Kim, Dae-Seok [1 ]
Kim, Kyung-Hee [2 ]
Yoo, Byong Chul [2 ]
Kim, Seok-Hyun [1 ]
Gong, Young-Dae [3 ]
Kim, Soo-Youl [1 ]
机构
[1] Natl Canc Ctr, Div Canc Biol, Canc Cell & Mol Biol Branch, Goyang 410769, Gyeonggi Do, South Korea
[2] Natl Canc Ctr, Colorectal Canc Branch, Div Translat & Clin Res 1, Res Inst, Goyang 410769, Gyeonggi Do, South Korea
[3] Dongguk Univ, Ctr Innovat Drug Lib Res, Seoul, South Korea
基金
新加坡国家研究基金会;
关键词
kidney cancer; autophagy; protein cross-linking; CROSS-LINKING ENZYMES; TISSUE TRANSGLUTAMINASE; CANCER-CELLS; SURVIVAL; DISEASE; PROTEIN; PATHWAY; COMPLEX; ALPHA;
D O I
10.1096/fj.12-224220
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Renal cell carcinoma (RCC), the predominant form of kidney cancer, is characterized by high resistance to radiation and chemotherapy. This study shows that expression of protein cross-linking enzyme transglutaminase 2 (TGase 2) is markedly increased in 7 renal cell carcinoma (RCC) cell lines in comparison to HEK293 and other cancer cell lines, such as NCI 60. However, the key role of TGase 2 in RCC was not clear. The down-regulation of TGase 2 was found to stabilize p53 expression, thereby inducing a 3- to 10-fold increase in apoptosis for 786-O, A498, CAKI-1, and ACHN cell lines by DAPI staining. MEF cells from TGase 2(-/-) mice showed stabilized p53 under apoptotic stress to compare to MEFs from wild-type mice. TGase 2 directly cross links the DNA binding domain of p53, leading to p53 depletion via autophagy in RCC. TGase 2 and p53 expression showed an inverse relationship in RCC cells. This finding implies that induced expression of TGase 2 promotes tumor cell survival through p53 depletion in RCC.Ku, B.M., Kim, D.-S. Kim, K.-H., Yoo, B.C., Kim, S.-H., Gong, Y.-D., Kim, S.-Y. Transglutaminase 2 inhibition found to induce p53 mediated apoptosis in renal cell carcinoma.
引用
收藏
页码:3487 / 3495
页数:9
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