Protocadherin 10 suppresses tumorigenesis and metastasis in colorectal cancer and its genetic loss predicts adverse prognosis

被引:36
作者
Jao, Tzu-Ming [1 ]
Tsai, Ming-Hong [2 ,3 ]
Lio, Hoi-Yan [1 ]
Weng, Wei-Ting [1 ]
Chen, Chun-Chieh [1 ]
Tzeng, Sheng-Tai [1 ]
Chang, Chia-Yun [1 ]
Lai, Yen-Chun [1 ]
Yen, Sou-Jhy [2 ]
Yu, Sung-Liang [1 ,4 ]
Yang, Ya-Chien [1 ,4 ]
机构
[1] Natl Taiwan Univ, Coll Med, Dept Clin Lab Sci & Med Biotechnol, Taipei 100, Taiwan
[2] Cardinal Tien Hosp, Dept Surg, New Taipei City, Taiwan
[3] Fu Jen Catholic Univ, Sch Med, New Taipei City, Taiwan
[4] Natl Taiwan Univ Hosp, Dept Lab Med, Taipei, Taiwan
关键词
PCDH10; colorectal cancer; loss of heterozygosity; prognostic marker; liver metastasis; CANDIDATE TUMOR-SUPPRESSOR; PCDH10 PROMOTER METHYLATION; MOLECULAR MARKERS; OL-PROTOCADHERIN; FREQUENT; DELETIONS; THERAPY; HYPERMETHYLATION; INSTABILITY; EXPRESSION;
D O I
10.1002/ijc.28899
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Protocadherin 10 (PCDH10), a novel tumor suppressor gene in human cancers, is located in a common deleted region at chromosome 4q28 in colorectal cancer (CRC). This study aimed to ascertain the genetic loss of PCDH10 and its clinical relevance in CRC and to explore the tumor suppressor function of PCDH10. The genetic deletion of PCDH10 was determined in 171 pairs of primary tumors and corresponding normal mucosae by loss of heterozygosity study. In total, 53 carcinomas were positive for allelic loss of PCDH10. The genetic aberration was significantly associated with tumor progression and distant metastasis (p=0.021 and p=0.018, respectively) and was an independent predictor of poor survival for CRC patients (p=0.005). Expression of PCDH10 gene was silenced or markedly down-regulated in all of 12 CRC cell lines tested and in 41 of 53 colorectal carcinomas compared with their matched normal mucosae. Ectopic expression of PCDH10 suppressed cancer cell proliferation, anchorage-independent growth, migration and invasion in vitro. Subcutaneous injection of PCDH10-expressing CRC cells into SCID mice revealed the reduction of tumor growth compared with that observed in mock-inoculated mice. Furthermore, through intrasplenic implantation, the re-expression of PCDH10 in silenced cells restrained liver metastasis and improved survival in SCID mice. In conclusion, PCDH10 is a pivotal tumor suppressor in CRC, and the loss of its function promotes not only tumor progression but also liver metastasis. In addition, the genetic deletion of PCDH10 represents an adverse prognostic marker for the survival of patients with CRC.
引用
收藏
页码:2593 / 2603
页数:11
相关论文
共 50 条
[21]   Molecular Origins of Cancer: Molecular Basis of Colorectal Cancer. [J].
Markowitz, Sanford D. ;
Bertagnolli, Monica M. .
NEW ENGLAND JOURNAL OF MEDICINE, 2009, 361 (25) :2449-2460
[22]   WebSat - A web software for microsatellite marker development [J].
Martins, Wellington Santos ;
Soares Lucas, Divino Cesar ;
de Souza Neves, Kelligton Fabricio ;
Bertioli, David John .
BIOINFORMATION, 2009, 3 (06) :282-283
[23]   Drug therapy - Systemic therapy for colorectal cancer [J].
Meyerhardt, JA ;
Mayer, RJ .
NEW ENGLAND JOURNAL OF MEDICINE, 2005, 352 (05) :476-487
[24]   Identifying autism loci and genes by tracing recent shared ancestry [J].
Morrow, Eric M. ;
Yoo, Seung-Yun ;
Flavell, Steven W. ;
Kim, Tae-Kyung ;
Lin, Yingxi ;
Hill, Robert Sean ;
Mukaddes, Nahit M. ;
Balkhy, Soher ;
Gascon, Generoso ;
Hashmi, Asif ;
Al-Saad, Samira ;
Ware, Janice ;
Joseph, Robert M. ;
Greenblatt, Rachel ;
Gleason, Danielle ;
Ertelt, Julia A. ;
Apse, Kira A. ;
Bodell, Adria ;
Partlow, Jennifer N. ;
Barry, Brenda ;
Yao, Hui ;
Markianos, Kyriacos ;
Ferland, Russell J. ;
Greenberg, Michael E. ;
Walsh, Christopher A. .
SCIENCE, 2008, 321 (5886) :218-223
[25]   Contact-dependent promotion of cell migration by the OL-protocadherin-Nap1 interaction [J].
Nakao, Shinsuke ;
Platek, Anna ;
Hirano, Shinji ;
Takeichi, Masatoshi .
JOURNAL OF CELL BIOLOGY, 2008, 182 (02) :395-410
[26]   PCDH10 Promoter Hypermethylation is Frequent in most Histologic Subtypes of Mature Lymphoid Malignancies and Occurs Early in Lymphomagenesis [J].
Narayan, Gopeshwar ;
Xie, Dongxu ;
Freddy, Allen J. ;
Ishdorj, Ganchimeg ;
Do, Catherine ;
Satwani, Prakash ;
Liyanage, Hema ;
Clark, Lorraine ;
Kisselev, Sergey ;
Nandula, Subhadra V. ;
Scotto, Luigi ;
Alobeid, Bachir ;
Savage, David ;
Tycko, Benjamin ;
O'Connor, Owen A. ;
Bhagat, Govind ;
Murty, Vundavalli V. .
GENES CHROMOSOMES & CANCER, 2013, 52 (11) :1030-1041
[27]   Promoter Methylation-Mediated Inactivation of PCDH10 in Acute Lymphoblastic Leukemia Contributes to Chemotherapy Resistance [J].
Narayan, Gopeshwar ;
Freddy, Allen J. ;
Xie, Dongxu ;
Liyanage, Hema ;
Clark, Lorraine ;
Kisselev, Sergey ;
Kang, Ji Un ;
Nandula, Subhadra V. ;
McGuinn, Catherine ;
Subramaniyam, Shivakumar ;
Alobeid, Bachir ;
Satwani, Prakash ;
Savage, David ;
Bhagat, Govind ;
Murty, Vundavalli V. .
GENES CHROMOSOMES & CANCER, 2011, 50 (12) :1043-1053
[28]   Protocadherin PCDH10, Involved in Tumor Progression, Is a Frequent and Early Target of Promoter Hypermethylation in Cervical Cancer [J].
Narayan, Gopeshwar ;
Scotto, Luigi ;
Neelakantan, Vijayalakshmi ;
Kottoor, Sherine H. ;
Wong, Ada Ho Yan ;
Loke, Shee-Loong ;
Mansukhani, Mahesh ;
Pothuri, Bhavana ;
Wright, Jason D. ;
Kaufmann, Andreas M. ;
Schneider, Achim ;
Arias-Pulido, Hugo ;
Tao, Qian ;
Murty, Vundavalli V. .
GENES CHROMOSOMES & CANCER, 2009, 48 (11) :983-992
[29]  
Perea J, 2011, REV ESP ENFERM DIG, V103, P29, DOI 10.4321/s1130-01082011000100006
[30]   δ-Protocadherins:: unique structures and functions [J].
Redies, C ;
Vanhalst, K ;
Roy, F .
CELLULAR AND MOLECULAR LIFE SCIENCES, 2005, 62 (23) :2840-2852