Limb-bud and Heart (LBH) Functions as a Tumor Suppressor of Nasopharyngeal Carcinoma by Inducing G1/S Cell Cycle Arrest

被引:35
作者
Liu, Qicai [1 ]
Guan, Xiaoying [2 ]
Lv, Jingli [1 ,3 ]
Li, Xiaoyan [4 ]
Wang, Yingfeng [1 ]
Li, Li [3 ]
机构
[1] Guangzhou Med Univ, Expt Med Res Ctr, Guangzhou 510182, Guangdong, Peoples R China
[2] Guangzhou Med Univ, Dept Pathol, Guangzhou 510182, Guangdong, Peoples R China
[3] Sun Yat Sen Univ, Ctr Canc, State Key Lab Oncol South China, Collaborat Innovat Ctr Canc Med, Guangzhou 510060, Guangdong, Peoples R China
[4] Sun Yat Sen Univ, Affiliated Hosp 1, Dept Nephrol, Guangzhou 510089, Guangdong, Peoples R China
关键词
ENCODED LATENT MEMBRANE-PROTEIN-1; TRANSFORMING GROWTH-FACTOR-BETA-1; COFACTOR LBH; GENE; EXPRESSION; GROWTH; POLYMORPHISM; D1; IDENTIFICATION; MICE;
D O I
10.1038/srep07626
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
Epstein-Barr virus-encoded latent membrane protein-1 (LMP1) plays a fundamental role in the malignant transformation of nasopharyngeal carcinoma (NPC), although the mechanism is not well understood. Here, we showed that Limb-bud and Heart (LBH) is considerably downregulated in patient NPC tissues. The expression of LBH in biopsies of 40 consecutive NPC patients devoid of initial distant metastasis and treated according to consistent guidelines was also analyzed, and we found the LBH expression level was correlated with some of clinicopathological features, disease-specific survival (DSS), distant metastasis-free survival (DMFS). We further determined that LBH normally induces NPC cell cycle arrest at the G1/S transition, and LBH can suppress the growth of transplanted NPC tumors in vivo by downregulating LMP1-mediated NF-kappa B transcriptional activity. Transforming growth factor-beta 1 (TGF-beta 1) normally protects against tumor development by suppressing cell proliferation, but NPC cells acquire resistance to TGF-beta 1-mediated inhibition. We found that TGF-beta 1 inhibits NF-kappa B transcriptional activity and nasopharyngeal epithelial cell proliferation through upregulating LBH expression. These data reveal a previously unknown NPC transformation mechanism and provide a new concept and treatment strategy for LMP1-driven oncogenesis in NPC.
引用
收藏
页数:10
相关论文
共 38 条
[1]
Biophysical characterization reveals structural disorder in the developmental transcriptional regulator LBH [J].
Al-Ali, Hassan ;
Rieger, Megan E. ;
Seldeen, Kenneth L. ;
Harris, Thomas K. ;
Farooq, Amjad ;
Briegel, Karoline J. .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2010, 391 (01) :1104-1109
[2]
TRAF interactions with raft-like buoyant complexes, better than TRAF rates of degradation, differentiate signaling by CD40 and EBV latent membrane protein 1 [J].
Ardila-Osorio, H ;
Pioche-Durieu, C ;
Puvion-Dutilleul, F ;
Clausse, B ;
Wiels, J ;
Miller, W ;
Raab-Traub, N ;
Busson, P .
INTERNATIONAL JOURNAL OF CANCER, 2005, 113 (02) :267-275
[3]
Congenital heart disease reminiscent of partial trisomy 2p syndrome in mice transgenic for the transcription factor Lbh [J].
Briegel, KJ ;
Baldwin, HS ;
Epstein, JA ;
Joyner, AL .
DEVELOPMENT, 2005, 132 (14) :3305-3316
[4]
Identification and characterization of Lbh, a novel conserved nuclear protein expressed during early limb and heart development [J].
Briegel, KJ ;
Joyner, AL .
DEVELOPMENTAL BIOLOGY, 2001, 233 (02) :291-304
[5]
The transcriptional cofactor Lbh regulates angiogenesis and endochondral bone formation during fetal bone development [J].
Conen, K. L. ;
Nishimori, S. ;
Provot, S. ;
Kronenberg, H. M. .
DEVELOPMENTAL BIOLOGY, 2009, 333 (02) :348-358
[6]
Polymorphisms of Toll-like receptor 9 are associated with nasopharyngeal carcinoma susceptibility [J].
Dai, Qiong ;
Li, Xing Pu ;
Chai, Li ;
Long, Han An ;
Yang, Zhi Hui .
TUMOR BIOLOGY, 2014, 35 (04) :3247-3253
[7]
ETIOLOGY OF NASOPHARYNGEAL CARCINOMA - A REVIEW [J].
HILDESHEIM, A ;
LEVINE, PH .
EPIDEMIOLOGIC REVIEWS, 1993, 15 (02) :466-485
[8]
Hinz M, 1999, MOL CELL BIOL, V19, P2690
[9]
Huang He, 2003, Ai Zheng, V22, P1254
[10]
Zheng H, 2007, CELL MOL IMMUNOL, V4, P185