HMGA2, but not HMGA1, is overexpressed in human larynx carcinomas

被引:21
作者
Palumbo, Antonio, Jr. [1 ,2 ]
De Martino, Marco [3 ]
Esposito, Francesco [3 ]
Fraggetta, Filippo [4 ]
Neto, Pedro N. [1 ]
Fernandes, Priscila Valverde [5 ]
Santos, Izabella C. [6 ]
Dias, Fernando L. [6 ]
Nasciutti, Luiz E. [2 ]
Da Costa, Nathalia Meireles [1 ]
Fusco, Alfredo [1 ,3 ]
Ribeiro Pinto, Luis Felipe [1 ]
机构
[1] Inst Nacl Canc INCA, Programa Carcinogenese Mol, Rio De Janeiro, Brazil
[2] Univ Fed Rio de Janeiro, Inst Ciencias Biomed, Lab Interacoes Celulares, Rio De Janeiro, Brazil
[3] Univ Naples Federico II, CNR, Ist Endocrinol & Oncol Sperimentale, Dipartimento Med Mol & Biotecnol Med,Scula Med &, Naples, Italy
[4] Osped Cannizzaro, Dept Pathol, Catania, Italy
[5] Inst Nacl Canc INCA, Div Patol, Rua Cordeiro Graca, Rio De Janeiro, Brazil
[6] Inst Nacl Canc INCA, Secao Cirurgia Cabeca & Pescoco, Rio De Janeiro, RJ, Brazil
关键词
carcinoma; HMGA pseudogenes; HMGA1; HMGA2; larynx; microRNA; SQUAMOUS-CELL CARCINOMA; GENE-EXPRESSION DATA; MOLECULAR-BIOLOGY; DOWN-REGULATION; NECK-CANCER; PROTEINS; HEAD; CONTRIBUTES; RADIOTHERAPY; PROGRESSION;
D O I
10.1111/his.13456
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Aims: Malignant tumours from the upper aerodigestive tract are grouped collectively in the class of head and neck squamous cell carcinoma (HNSCC). The head and neck tumours were responsible for more than 500000 cancer cases in 2012, accounting for the sixth highest incidence rate and mortality worldwide among all tumour types. Laryngeal squamous cell carcinoma (LSCC) possesses the second highest incidence rate among all HNSCC. Despite significant advances in surgery and radiotherapy during the last few decades, no treatment has been shown to achieve a satisfactory therapeutic outcome and the mortality rate of LSCC is still high, with a 5-year survival rate of 64%. Therefore, further investigations are required to identify the pathogenesis of LSCC. Methods and results: In order to search for new LSCC biomarkers, we have analysed the expression of the HMGA family members, HMGA1 and HMGA2, by quantitative reverse transcription-polymerase chain reaction (qRT-PCR) and immunohistochemistry. HMGA proteins are usually absent in the healthy adult tissues. In contrast, their constitutive expression is a feature of several neoplasias, being associated with a highly malignant phenotype and reduced survival. Here, we report HMGA2 overexpression in larynx carcinomas. Conversely, HMGA1 does not show any differences in its expression between normal and carcinoma tissues. Interestingly, HMGA2 overexpression appears associated with that of two HMGA1-pseudogenes, HMGA1P6 and HMGA1P7, acting as a sponge for HMGA1- and HMGA2-targeting microRNAs and involved in several human cancers. Conclusions: Therefore, HMGA2 overexpression appears to be a strong feature of larynx carcinoma, supporting its detection as a valid tool for the diagnosis of these malignancies.
引用
收藏
页码:1102 / 1114
页数:13
相关论文
共 40 条
[1]   An increased high-mobility group A2 expression level is associated with malignant phenotype in pancreatic exocrine tissue [J].
Abe, N ;
Watanabe, T ;
Suzuki, Y ;
Matsumoto, N ;
Masaki, T ;
Mori, T ;
Sugiyama, M ;
Chiappetta, G ;
Fusco, A ;
Atomi, Y .
BRITISH JOURNAL OF CANCER, 2003, 89 (11) :2104-2109
[2]   The impact of treatment center on the outcome of patients with laryngeal cancer treated with surgery and radiotherapy [J].
Akman, Fadime Can ;
Dag, Nihal ;
Ataman, Ozlem Uruk ;
Ecevit, Cenk ;
Ikiz, Ahmet Omer ;
Arslan, Isin ;
Sarioglu, Sulen ;
Ada, Emel ;
Kinay, Munir .
EUROPEAN ARCHIVES OF OTO-RHINO-LARYNGOLOGY, 2008, 265 (10) :1245-1255
[3]   Expression of the high mobility group proteins HMGI(Y) correlates with malignant progression in Barrett's metaplasia [J].
Chen, XY ;
Lechago, J ;
Ertan, A ;
Ergun, G ;
Verm, R ;
Bridges, M ;
Johnson, C ;
Woods, K ;
Meriano, F ;
Chirala, M ;
Younes, M .
CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION, 2004, 13 (01) :30-33
[4]   HMGA1 protein overexpression in human breast carcinomas: Correlation with ErbB2 expression [J].
Chiappetta, G ;
Botti, G ;
Monaco, M ;
Pasquinelli, R ;
Pentimalli, F ;
Di Bonito, M ;
D'Aiuto, G ;
Fedele, M ;
Iuliano, R ;
Palmieri, EA ;
Pierantoni, GM ;
Giancotti, V ;
Fusco, A .
CLINICAL CANCER RESEARCH, 2004, 10 (22) :7637-7644
[5]   The impairment of the High Mobility Group A (HMGA) protein function contributes to the anticancer activity of trabectedin [J].
D'Angelo, Daniela ;
Borbone, Eleonora ;
Palmieri, Dario ;
Uboldi, Sarah ;
Esposito, Francesco ;
Frapolli, Roberta ;
Pacelli, Roberto ;
D'Incalci, Maurizio ;
Fusco, Alfredo .
EUROPEAN JOURNAL OF CANCER, 2013, 49 (05) :1142-1151
[6]   Altered MicroRNA Expression Profile in Human Pituitary GH Adenomas: Down-Regulation of miRNA Targeting HMGA1, HMGA2, and E2F1 [J].
D'Angelo, Daniela ;
Palmieri, Dario ;
Mussnich, Paula ;
Roche, Magali ;
Wierinckx, Anne ;
Raverot, Gerald ;
Fedele, Monica ;
Croce, Carlo Maria ;
Trouillas, Jacqueline ;
Fusco, Alfredo .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2012, 97 (07) :E1128-E1138
[7]   RETRACTED: HMGA Proteins Up-regulate CCNB2 Gene in Mouse and Human Pituitary Adenomas (Retracted article. See vol. 78, pg. 6906, 2018) [J].
De Martino, Ivana ;
Visone, Rosa ;
Wierinckx, Anne ;
Palmieri, Dario ;
Ferraro, Angelo ;
Cappabianca, Paolo ;
Chiappetta, Gennaro ;
Forzati, Floriana ;
Lombardi, Gaetano ;
Colao, Annamaria ;
Trouillas, Jacqueline ;
Fedele, Monica ;
Fusco, Alfredo .
CANCER RESEARCH, 2009, 69 (05) :1844-1850
[8]   HMGA1P7-pseudogene regulates H19 and Igf2 expression by a competitive endogenous RNA mechanism [J].
De Martino, Marco ;
Forzati, Floriana ;
Marfella, Marianna ;
Pellecchia, Simona ;
Arra, Claudio ;
Terracciano, Luigi ;
Fusco, Alfredo ;
Esposito, Francesco .
SCIENTIFIC REPORTS, 2016, 6
[9]   HMGA1-pseudogenes and cancer [J].
De Martino, Marco ;
Forzati, Floriana ;
Arra, Claudio ;
Fusco, Alfredo ;
Esposito, Francesco .
ONCOTARGET, 2016, 7 (19) :28724-28735
[10]   Wanderer, an interactive viewer to explore DNA methylation and gene expression data in human cancer [J].
Diez-Villanueva, Anna ;
Mallona, Izaskun ;
Peinado, Miguel A. .
EPIGENETICS & CHROMATIN, 2015, 8