Literature DB >> 20177404

Mismatch repair deficient colorectal cancer in the era of personalized treatment.

Madeleine Hewish1, Christopher J Lord, Sarah A Martin, David Cunningham, Alan Ashworth.   

Abstract

The molecular and genetic subtyping of cancer has allowed the emergence of individualized therapies. This approach could potentially deliver treatments that have both increased efficacy as well as reduced toxicity. A well-defined subtype of colorectal cancer (CRC) is characterized by a deficiency in the mismatch repair (MMR) pathway. MMR deficiency not only contributes to the pathogenesis of a large proportion of CRC, but also determines the response to many of the drugs that are frequently used to treat this disease. In this Review we describe the MMR deficient phenotype and discuss how a deficiency in this DNA repair process may impact on the management of CRC, including surgery, adjuvant chemotherapy and the choice of systemic agents for the palliation of advanced disease. We also discuss how the DNA repair defect in MMR deficient CRC could be exploited in the development of novel therapeutic strategies.

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Year:  2010        PMID: 20177404     DOI: 10.1038/nrclinonc.2010.18

Source DB:  PubMed          Journal:  Nat Rev Clin Oncol        ISSN: 1759-4774            Impact factor:   66.675


  134 in total

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2.  BRAF mutation predicts sensitivity to MEK inhibition.

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4.  Incorporation of somatic BRAF mutation testing into an algorithm for the investigation of hereditary non-polyposis colorectal cancer.

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Review 5.  Drug resistance reversal--are we getting closer?

Authors:  R D Baird; S B Kaye
Journal:  Eur J Cancer       Date:  2003-11       Impact factor: 9.162

6.  Association between DNA methylation and shortened survival in patients with advanced colorectal cancer treated with 5-fluorouracil based chemotherapy.

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7.  Prognostic significance of defective mismatch repair and BRAF V600E in patients with colon cancer.

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Journal:  Gut       Date:  2002-10       Impact factor: 23.059

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  83 in total

1.  MicroRNA-21 induces resistance to 5-fluorouracil by down-regulating human DNA MutS homolog 2 (hMSH2).

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Journal:  Proc Natl Acad Sci U S A       Date:  2010-11-15       Impact factor: 11.205

2.  Inactivation of DNA mismatch repair by variants of uncertain significance in the PMS2 gene.

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4.  DNA mismatch repair proficiency executing 5-fluorouracil cytotoxicity in colorectal cancer cells.

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Journal:  Cancer Biol Ther       Date:  2011-10-15       Impact factor: 4.742

5.  EGFR inhibits DNA mismatch repair.

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Review 6.  Postreplicative mismatch repair.

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Review 7.  Colorectal cancer with liver metastases: neoadjuvant chemotherapy, surgical resection first or palliation alone?

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Journal:  World J Gastroenterol       Date:  2014-09-21       Impact factor: 5.742

Review 8.  Biomarkers for immune therapy in colorectal cancer: mismatch-repair deficiency and others.

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10.  MicroRNA-31-5p modulates cell cycle by targeting human mutL homolog 1 in human cancer cells.

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