MicroRNA 183 family profiles in pheochromocytomas are related to clinical parameters and SDHB expression

被引:7
作者
Pillai, Suja [1 ,2 ]
Lo, Chung Y. [3 ]
Liew, Victor [4 ]
Lalloz, Minella [1 ,2 ]
Smith, Robert A. [1 ,2 ,5 ]
Gopalan, Vinod [1 ,2 ]
Lam, Alfred King-Yin [1 ,2 ]
机构
[1] Griffith Univ, Sch Med, Canc Mol Pathol, Gold Coast 4222, Australia
[2] Griffith Univ, Menzies Hlth Inst Queensland, Gold Coast 4222, Australia
[3] Univ Hong Kong, Li Ka Shing Fac Med, Dept Surg, Hong Kong, Hong Kong, Peoples R China
[4] Gold Coast Private Hosp, Dept Surg, Southport, Qld 4215, Australia
[5] Queensland Univ Technol, Inst Hlth & Biomed Innovat, Genom Res Ctr, Kelvin Grove, Qld 4059, Australia
关键词
MicroRNA-183; cluster; Pheochromocytoma; Sporadic; SDHB; Adrenal; BENIGN; CANCER; OVEREXPRESSION; PARAGANGLIOMAS; PROLIFERATION; HEREDITARY; MALIGNANCY; MIGRATION; CELLS; GENE;
D O I
10.1016/j.humpath.2017.03.017
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
This study aims to examine the expression profiles of the miR-183 cluster (miR-96/182/183) in pheochromocytoma. Pheochromocytoma tissues were prospectively collected from 50 patients with pheochromocytoma. Expression of miR-183 cluster members and SDHB protein expression were analyzed in these tissues by quantitative real-time polymerase chain reaction and immunohistochemistry, respectively. The expression of miR-183 cluster members in pheochromocytomas was correlated with the clinical and pathological parameters of these patients. The expression levels of miR-183 cluster members were predominantly downregulated or deleted in pheochromocytoma. Low expression or deletion of miR-96 was predominantly noted in younger patients with pheochromocytoma (<50 years, P =.01). Female patients in the study group showed marked deletion of miR-182 (P = .05). Deletion of the cluster was also associated with SDHB protein expression in pheochromocytoma. Moreover, patients with low miR-183 cluster expression had a slightly better survival rate when compared with patients with high expression. To conclude, the findings indicate a role for miR-183 cluster members in the pathogenesis and clinical progression of pheochromocytoma. (C) 2017 Elsevier Inc. All rights reserved.
引用
收藏
页码:91 / 97
页数:7
相关论文
共 37 条
[1]   Adrenal tumours are more predominant in females regardless of their histological subtype: a review [J].
Audenet, Francois ;
Mejean, Arnaud ;
Chartier-Kastler, Emmanuel ;
Roupret, Morgan .
WORLD JOURNAL OF UROLOGY, 2013, 31 (05) :1037-1043
[2]   CGH and C 44/MIB-1 immunohistochemistry are helpful to distinguish metastasized from nonmetastasized sporadic pheochromocytomas [J].
August, C ;
August, K ;
Schroeder, S ;
Bahn, H ;
Hinze, R ;
Baba, HA ;
Kersting, C ;
Buerger, H .
MODERN PATHOLOGY, 2004, 17 (09) :1119-1128
[3]   SDHB loss predicts malignancy in pheochromocytomas/sympathethic paragangliomas, but not through hypoxia signalling [J].
Blank, Annika ;
Schmitt, Anja M. ;
Korpershoek, Esther ;
van Nederveen, Francien ;
Rudolph, Thomas ;
Weber, Nicole ;
Strebel, Raeto Thomas ;
de Krijger, Ronald ;
Komminoth, Paul ;
Perren, Aurel .
ENDOCRINE-RELATED CANCER, 2010, 17 (04) :919-928
[4]   Multi-omics analysis defines core genomic alterations in pheochromocytomas and paragangliomas [J].
Castro-Vega, Luis Jaime ;
Letouze, Eric ;
Burnichon, Nelly ;
Buffet, Alexandre ;
Disderot, Pierre-Helie ;
Khalifa, Emmanuel ;
Loriot, Celine ;
Elarouci, Nabila ;
Morin, Aurelie ;
Menara, Melanie ;
Lepoutre-Lussey, Charlotte ;
Badoual, Cecile ;
Sibony, Mathilde ;
Dousset, Bertrand ;
Libe, Rossella ;
Zinzindohoue, Franck ;
Plouin, Pierre Francois ;
Bertherat, Jerome ;
Amar, Laurence ;
de Reynies, Aurelien ;
Favier, Judith ;
Gimenez-Roqueplo, Anne-Paule .
NATURE COMMUNICATIONS, 2015, 6
[5]   Novel pheochromocytoma susceptibility loci identified by integrative genomics [J].
Dahia, PLM ;
Hao, K ;
Rogus, J ;
Colin, C ;
Pujana, MAG ;
Ross, K ;
Magoffin, D ;
Aronin, N ;
Cascon, A ;
Hayashida, CY ;
Li, C ;
Toledo, SPA ;
Stiles, CD .
CANCER RESEARCH, 2005, 65 (21) :9651-9658
[6]   The microRNA-183 cluster: the family that plays together stays together [J].
Dambal, Shweta ;
Shah, Mit ;
Mihelich, Brittany ;
Nonn, Larisa .
NUCLEIC ACIDS RESEARCH, 2015, 43 (15) :7173-7188
[7]   Integrative analysis of miRNA and mRNA expression profiles in pheochromocytoma and paraganglioma identifies genotype-specific markers and potentially regulated pathways [J].
de Cubas, Aguirre A. ;
Javier Leandro-Garcia, L. ;
Schiavi, Francesca ;
Mancikova, Veronika ;
Comino-Mendez, Inaki ;
Inglada-Perez, Lucia ;
Perez-Martinez, Manuel ;
Ibarz, Nuria ;
Ximenez-Embun, Pilar ;
Lopez-Jimenez, Elena ;
Maliszewska, Agnieszka ;
Leton, Rocio ;
Gomez Grana, Alvaro ;
Bernal, Carmen ;
Alvarez-Escola, Cristina ;
Rodriguez-Antona, Cristina ;
Opocher, Giuseppe ;
Munoz, Javier ;
Megias, Diego ;
Cascon, Alberto ;
Robledo, Mercedes .
ENDOCRINE-RELATED CANCER, 2013, 20 (04) :477-493
[8]   Rationale for Anti-angiogenic Therapy in Pheochromocytoma and Paraganglioma [J].
Favier, Judith ;
Igaz, Peter ;
Burnichon, Nelly ;
Amar, Laurence ;
Libe, Rossella ;
Badoual, Cecile ;
Tissier, Frederique ;
Bertherat, Jerome ;
Plouin, Pierre-Francois ;
Jeunemaitre, Xavier ;
Gimenez-Roqueplo, Anne-Paule .
ENDOCRINE PATHOLOGY, 2012, 23 (01) :34-42
[9]   Downregulation of microRNA-498 in colorectal cancers and its cellular effects [J].
Gopalan, Vinod ;
Smith, Robert A. ;
Lam, Alfred K. -Y. .
EXPERIMENTAL CELL RESEARCH, 2015, 330 (02) :423-428
[10]   Regulation of microRNA-1288 in Colorectal Cancer: Altered Expression and Its Clinicopathological Significance [J].
Gopalan, Vinod ;
Pillai, Suja ;
Ebrahimi, Faeza ;
Salajegheh, Ali ;
Lam, Tommy C. ;
Le, Tran K. ;
Langsford, Nicole ;
Ho, Yik-Hong ;
Smith, Robert A. ;
Lam, Alfred K. -Y. .
MOLECULAR CARCINOGENESIS, 2014, 53 :E36-E44