HMGA1-pseudogenes and cancer

被引:32
作者
De Martino, Marco [1 ]
Forzati, Floriana [1 ]
Arra, Claudio [2 ]
Fusco, Alfredo [1 ]
Esposito, Francesco [1 ]
机构
[1] Univ Naples Federico II, Scuola Med & Chirurg Napoli, Dipartimento Med Mol & Biotecnol Med, Ist Endocrinol & Oncol Sperimentale,CNR, Naples, Italy
[2] Fdn Pascale, Ist Nazl Tumori, Naples, Italy
关键词
pseudogenes; HMGA; cancer; ceRNA; MOBILITY-GROUP PROTEINS; GROUP A1 PROTEINS; GENE-EXPRESSION; HMGA PROTEINS; PSEUDOGENES PSEUDO; OVARIAN-CARCINOMA; TUMOR-CELLS; AT-HOOK; BREAST; MICRORNAS;
D O I
10.18632/oncotarget.7427
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Pseudogenes are DNA sequences with high homology to the corresponding functional gene, but, because of the accumulation of various mutations, they have lost their initial functions to code for proteins. Consequently, pseudogenes have been considered until few years ago dysfunctional relatives of the corresponding ancestral genes, and then useless in the course of genome evolution. However, several studies have recently established that pseudogenes are owners of key biological functions. Indeed, some pseudogenes control the expression of functional genes by competitively binding to the miRNAs, some of them generate small interference RNAs to negatively modulate the expression of functional genes, and some of them even encode functional mutated proteins. Here, we concentrate our attention on the pseudogenes of the HMGA1 gene, that codes for the HMGA1a and HMGA1b proteins having a critical role in development and cancer progression. In this review, we analyze the family of HMGA1 pseudogenes through three aspects: classification, characterization, and their possible function and involvement in cancer.
引用
收藏
页码:28724 / 28735
页数:12
相关论文
共 118 条
[1]  
Abe N, 1999, CANCER RES, V59, P1169
[2]   HMGA1 Is Induced by Wnt/β-Catenin Pathway and Maintains Cell Proliferation in Gastric Cancer [J].
Akaboshi, Shin-ichi ;
Watanabe, Sugiko ;
Hino, Yuko ;
Sekita, Yoko ;
Xi, Yang ;
Araki, Kimi ;
Yamamura, Ken-ichi ;
Oshima, Masanobu ;
Ito, Takaaki ;
Baba, Hideo ;
Nakao, Mitsuyoshi .
AMERICAN JOURNAL OF PATHOLOGY, 2009, 175 (04) :1675-1685
[3]   Pseudogenes: Are they "Junk" or functional DNA? [J].
Balakirev, ES ;
Ayala, FJ .
ANNUAL REVIEW OF GENETICS, 2003, 37 :123-151
[4]   MicroRNAs: Genomics, biogenesis, mechanism, and function (Reprinted from Cell, vol 116, pg 281-297, 2004) [J].
Bartel, David P. .
CELL, 2007, 131 (04) :11-29
[5]   HMGA1 Induces Intestinal Polyposis in Transgenic Mice and Drives Tumor Progression and Stem Cell Properties in Colon Cancer Cells [J].
Belton, Amy ;
Gabrovsky, Alexander ;
Bae, Young Kyung ;
Reeves, Ray ;
Iacobuzio-Donahue, Christine ;
Huso, David L. ;
Resar, Linda M. S. .
PLOS ONE, 2012, 7 (01)
[6]   Thyroid cell transformation requires the expression of the HMGA1 proteins [J].
Berlingieri, MT ;
Pierantoni, GM ;
Giancotti, V ;
Santoro, M ;
Fusco, A .
ONCOGENE, 2002, 21 (19) :2971-2980
[7]   Proneural genes and the specification of neural cell types [J].
Bertrand, N ;
Castro, DS ;
Guillemot, F .
NATURE REVIEWS NEUROSCIENCE, 2002, 3 (07) :517-530
[8]   Recent advances in the molecular genetics of type 2 diabetes mellitus [J].
Brunetti, Antonio ;
Chiefari, Eusebio ;
Foti, Daniela .
WORLD JOURNAL OF DIABETES, 2014, 5 (02) :128-140
[9]   The Wnt/β-catenin/T-cell factor 4 pathway up-regulates high-mobility group A1 expression in colon cancer [J].
Bush, Bethany M. ;
Brock, Ashton T. ;
Deng, Jiayue A. ;
Nelson, Ronald A. ;
Sumter, Takita Felder .
CELL BIOCHEMISTRY AND FUNCTION, 2013, 31 (03) :228-236
[10]   MicroRNA signatures in human cancers [J].
Calin, George A. ;
Croce, Carlo M. .
NATURE REVIEWS CANCER, 2006, 6 (11) :857-866