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
相关论文
共 26 条
[11]  
Kawasaki T, 1999, ONCOL REP, V6, P329
[12]   Cancer cells promote survival through depletion of the von Hippel-Lindau tumor suppressor by protein crosslinking [J].
Kim, D-S ;
Choi, Y-B ;
Han, B-G ;
Park, S-Y ;
Jeon, Y. ;
Kim, D-H ;
Ahn, E-R ;
Shin, J-E ;
Lee, B. I. ;
Lee, H. ;
Hong, K-M ;
Kim, S-Y .
ONCOGENE, 2011, 30 (48) :4780-4790
[13]   Reversal of drug resistance in breast cancer cells by transglutaminase 2 inhibition and nuclear factor-κB inactivation [J].
Kim, Dae-Seok ;
Park, Sung-Soo ;
Nam, Byung-Ho ;
Kim, In-Hoo ;
Kim, Soo-Youl .
CANCER RESEARCH, 2006, 66 (22) :10936-10943
[14]   Transglutaminase 2 gene ablation protects against renal ischemic injury by blocking constant NF-κB activation [J].
Kim, Dae-Seok ;
Kim, Bora ;
Tahk, Hongmin ;
Kim, Dong-Hyun ;
Ahn, Eu-Ree ;
Choi, Changsun ;
Jeon, Yoon ;
Park, Seo Young ;
Lee, Ho ;
Oh, Seung Hyun ;
Kim, Soo-Youl .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2010, 403 (3-4) :479-484
[15]   Depletion of cathepsin D by transglutaminase 2 through protein cross-linking promotes cell survival [J].
Kim, Se-Jin ;
Kim, Kyung-Hee ;
Ahn, Eu-Ree ;
Yoo, Byong Chul ;
Kim, Soo-Youl .
AMINO ACIDS, 2013, 44 (01) :73-80
[16]   Modes of p53 Regulation [J].
Kruse, Jan-Philipp ;
Gu, Wei .
CELL, 2009, 137 (04) :609-622
[17]   Transglutaminase 2 induces nuclear factor-κB activation via a novel pathway in BV-2 microglia [J].
Lee, JM ;
Kim, YS ;
Choi, DH ;
Bang, MS ;
Han, TR ;
Joh, TH ;
Kim, SY .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (51) :53725-53735
[18]  
Lipworth L, 2006, J UROLOGY, V176, P2353, DOI 10.1016/j.juro.2006.07.130
[19]   Transglutaminases: Crosslinking enzymes with pleiotropic functions [J].
Lorand, L ;
Graham, RM .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2003, 4 (02) :140-156
[20]   'Tissue' transglutaminase ablation reduces neuronal death and prolongs survival in a mouse model of Huntington's disease [J].
Mastroberardino, P ;
Iannicola, C ;
Nardacci, R ;
Bernassola, F ;
De Laurenzi, V ;
Melino, G ;
Moreno, S ;
Pavone, F ;
Oliverio, S ;
Fesus, L ;
Piacentini, M .
CELL DEATH AND DIFFERENTIATION, 2002, 9 (09) :873-880