Characterization of MTAP Gene Expression in Breast Cancer Patients and Cell Lines

被引:20
作者
Vieira de Oliveira, Sarah Franco [1 ]
Ganzinelli, Monica [2 ]
Chila, Rosaria [2 ]
Serino, Leandro [1 ]
Maciel, Marcos Euzebio [1 ]
Urban, Cicero de Andrade [3 ]
de Lima, Rubens Silveira [3 ]
Cavalli, Iglenir Joao [1 ]
Generali, Daniele [4 ]
Broggini, Massimo [2 ]
Damia, Giovanna [2 ]
de Souza Fonseca Ribeiro, Enilze Maria [1 ]
机构
[1] Univ Fed Parana, Dept Genet, BR-80060000 Curitiba, Parana, Brazil
[2] Ist Ric Farmacol Mario Negri, Dept Oncol, Mol Pharmacol Lab, Milan, Lombardia, Italy
[3] Hosp Nossa Senhora Gracas, Dept Mastol, Breast Unit, Curitiba, Parana, Brazil
[4] AO Ist Ospitalieri Cremona, UO Multidisciplinare Patol Mammaria, Lab Oncol Mol Senol, Cremona, Lombardia, Italy
关键词
METHYLTHIOADENOSINE PHOSPHORYLASE MTAP; HOMOZYGOUS DELETION; DOWN-REGULATION; CONCORDANT LOSS; 6-THIOGUANINE; DEFICIENT; CARCINOMA; TUMORS;
D O I
10.1371/journal.pone.0145647
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
07 ; 0710 ; 09 ;
摘要
MTAP is a ubiquitously expressed gene important for adenine and methionine salvage. The gene is located at 9p21, a chromosome region often deleted in breast carcinomas, similar to CDKN2A, a recognized tumor suppressor gene. Several research groups have shown that MTAP acts as a tumor suppressor, and some therapeutic approaches were proposed based on a tumors 'MTAP status. We analyzed MTAP and CDKN2A gene (RT-qPCR) and protein (western-blotting) expression in seven breast cancer cell lines and evaluated their promoter methylation patterns to better characterize the contribution of these genes to breast cancer. Cytotoxicity assays with inhibitors of de novo adenine synthesis (5-FU, AZA and MTX) after MTAP gene knockdown showed an increased sensitivity, mainly to 5-FU. MTAP expression was also evaluated in two groups of samples from breast cancer patients, fresh tumors and paired normal breast tissue, and from formalin-fixed paraffin embedded (FFPE) core breast cancer samples diagnosed as Luminal-A tumors and triple negative breast tumors (TNBC). The difference of MTAP expression between fresh tumors and normal tissues was not statistically significant. However, MTAP expression was significantly higher in Luminal-A breast tumors than in TNBC, suggesting the lack of expression in more aggressive breast tumors and the possibility of using the new approaches based on MTAP status in TNBC.
引用
收藏
页数:13
相关论文
共 33 条
[1]  
Alhebshi HM, 2008, ASIAN PAC J CANCER P, V9, P291
[2]  
[Anonymous], 2018, ANTI-CANCER DRUG, DOI [DOI 10.3322/caac.20115, DOI 10.1097/CAD.0000000000000617]
[3]   Targeting tumors that lack methylthioadenosine phosphorylase (MTAP) activity Current strategies [J].
Bertino, Joseph R. ;
Waud, William R. ;
Parker, William B. ;
Lubin, Martin .
CANCER BIOLOGY & THERAPY, 2011, 11 (07) :627-632
[4]   Molecular analysis of the INK4A and INK4B gene loci in human breast cancer cell lines and primary carcinomas [J].
Bisogna, M ;
Calvano, JE ;
Ho, GH ;
Orlow, I ;
Cordón-Cardó, C ;
Borgen, PI ;
Van Zee, KJ .
CANCER GENETICS AND CYTOGENETICS, 2001, 125 (02) :131-138
[5]   Basal-like breast cancer defined by five biomarkers has superior prognostic value then triple-negative phenotype [J].
Cheang, Maggie C. U. ;
Voduc, David ;
Bajdik, Chris ;
Leung, Samuel ;
McKinney, Steven ;
Chia, Stephen K. ;
Perou, Charles M. ;
Nielsen, Torsten O. .
CLINICAL CANCER RESEARCH, 2008, 14 (05) :1368-1376
[6]   Expression of methylthioadenosine phosphorylase cDNA in p16(-), MTAP(-) malignant cells: Restoration of methylthioadenosine phosphorylase-dependent salvage pathways and alterations of sensitivity to inhibitors of purine de novo synthesis [J].
Chen, ZH ;
Olopade, OI ;
Savarese, TM .
MOLECULAR PHARMACOLOGY, 1997, 52 (05) :903-911
[7]  
Christopher SA, 2002, CANCER RES, V62, P6639
[8]   Methylthioadenosine phosphorylase inactivation depends on gene deletion in laryngeal squamous cell carcinoma [J].
Conde, Laura ;
Vilaseca, Isabel ;
Alos, Llucia ;
Bernal-Sprekelsen, Manuel ;
Cardesa, Antonio ;
Nadal, Alfons .
HISTOPATHOLOGY, 2012, 61 (06) :1082-1088
[9]   Amplified and Homozygously Deleted Genes in Glioblastoma: Impact on Gene Expression Levels [J].
Crespo, Ines ;
Tao, Herminio ;
Belen Nieto, Ana ;
Rebelo, Olinda ;
Domingues, Patricia ;
Vital, Ana Luisa ;
del Carmen Patino, Maria ;
Barbosa, Marcos ;
Lopes, Maria Celeste ;
Oliveira, Catarina Resende ;
Orfao, Alberto ;
Dolores Tabernero, Maria .
PLOS ONE, 2012, 7 (09)
[10]   The genomic and transcriptomic architecture of 2,000 breast tumours reveals novel subgroups [J].
Curtis, Christina ;
Shah, Sohrab P. ;
Chin, Suet-Feung ;
Turashvili, Gulisa ;
Rueda, Oscar M. ;
Dunning, Mark J. ;
Speed, Doug ;
Lynch, Andy G. ;
Samarajiwa, Shamith ;
Yuan, Yinyin ;
Graef, Stefan ;
Ha, Gavin ;
Haffari, Gholamreza ;
Bashashati, Ali ;
Russell, Roslin ;
McKinney, Steven ;
Langerod, Anita ;
Green, Andrew ;
Provenzano, Elena ;
Wishart, Gordon ;
Pinder, Sarah ;
Watson, Peter ;
Markowetz, Florian ;
Murphy, Leigh ;
Ellis, Ian ;
Purushotham, Arnie ;
Borresen-Dale, Anne-Lise ;
Brenton, James D. ;
Tavare, Simon ;
Caldas, Carlos ;
Aparicio, Samuel .
NATURE, 2012, 486 (7403) :346-352