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Alternative Splicing as a Target for Cancer Treatment
被引:87
作者:

Martinez-Montiel, Nancy
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机构:
Benemerita Univ Autonoma Puebla, Inst Ciencias, Ctr Invest Ciencias Microbiol, Puebla 72470, Mexico
Univ Sherbrooke, Dept Microbiol & Infect Dis, Fac Med & Hlth Sci, Sherbrooke, PQ J1E 4K8, Canada Benemerita Univ Autonoma Puebla, Inst Ciencias, Ctr Invest Ciencias Microbiol, Puebla 72470, Mexico

Rosas-Murrieta, Nora Hilda
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Benemerita Univ Autonoma Puebla, Fac Ciencias Quim, Puebla 72470, Mexico Benemerita Univ Autonoma Puebla, Inst Ciencias, Ctr Invest Ciencias Microbiol, Puebla 72470, Mexico

Anaya Ruiz, Maricruz
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机构:
IMSS, Ctr Invest Biomed Oriente CIBIOR, Puebla 74360, Mexico Benemerita Univ Autonoma Puebla, Inst Ciencias, Ctr Invest Ciencias Microbiol, Puebla 72470, Mexico

Monjaraz-Guzman, Eduardo
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h-index: 0
机构:
Benemerita Univ Autonoma Puebla, Inst Fisiol, Puebla 72470, Mexico Benemerita Univ Autonoma Puebla, Inst Ciencias, Ctr Invest Ciencias Microbiol, Puebla 72470, Mexico

Martinez-Contreras, Rebeca
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Benemerita Univ Autonoma Puebla, Inst Ciencias, Ctr Invest Ciencias Microbiol, Puebla 72470, Mexico Benemerita Univ Autonoma Puebla, Inst Ciencias, Ctr Invest Ciencias Microbiol, Puebla 72470, Mexico
机构:
[1] Benemerita Univ Autonoma Puebla, Inst Ciencias, Ctr Invest Ciencias Microbiol, Puebla 72470, Mexico
[2] Univ Sherbrooke, Dept Microbiol & Infect Dis, Fac Med & Hlth Sci, Sherbrooke, PQ J1E 4K8, Canada
[3] Benemerita Univ Autonoma Puebla, Fac Ciencias Quim, Puebla 72470, Mexico
[4] IMSS, Ctr Invest Biomed Oriente CIBIOR, Puebla 74360, Mexico
[5] Benemerita Univ Autonoma Puebla, Inst Fisiol, Puebla 72470, Mexico
关键词:
alternative splicing;
cancer;
diagnosis;
therapeutics;
PRE-MESSENGER-RNA;
CHRONIC LYMPHOCYTIC-LEUKEMIA;
CYCLIN D1;
BREAST-CANCER;
TUMOR-SUPPRESSOR;
PREMESSENGER RNA;
ANTICANCER DRUG;
IN-VITRO;
ANTISENSE OLIGONUCLEOTIDES;
ANTITUMOR-ACTIVITY;
D O I:
10.3390/ijms19020545
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Alternative splicing is a key mechanism determinant for gene expression in metazoan. During alternative splicing, non-coding sequences are removed to generate different mature messenger RNAs due to a combination of sequence elements and cellular factors that contribute to splicing regulation. A different combination of splicing sites, exonic or intronic sequences, mutually exclusive exons or retained introns could be selected during alternative splicing to generate different mature mRNAs that could in turn produce distinct protein products. Alternative splicing is the main source of protein diversity responsible for 90% of human gene expression, and it has recently become a hallmark for cancer with a full potential as a prognostic and therapeutic tool. Currently, more than 15,000 alternative splicing events have been associated to different aspects of cancer biology, including cell proliferation and invasion, apoptosis resistance and susceptibility to different chemotherapeutic drugs. Here, we present well established and newly discovered splicing events that occur in different cancer-related genes, their modification by several approaches and the current status of key tools developed to target alternative splicing with diagnostic and therapeutic purposes.
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