Literature DB >> 20571907

PIK3CA mutations in KRAS and BRAF wild type colorectal cancer patients. A study of Spanish population.

Marta Herreros-Villanueva1, Noemí Gomez-Manero, Pilar Muñiz, Carlos García-Girón, Maria Jesús Coma del Corral.   

Abstract

The objective of the work was to study PIK3CA mutations in wild type KRAS and BRAF colorectal cancer. Clinicopathological data and paraffin-embedded specimens were collected on 73 patients who underwent colorectal resections at General Yagüe Hospital in Burgos. KRAS, BRAF and PIK3CA status were analyzed by real-time PCR in all patients. PIK3CA mutations were present in 8.22% of wild type KRAS and BRAF colorectal cancers. The most frequent mutation is E545K/D in exon 9 which represents 83.3% of all mutations. By contrast, we did not found any tumour harbouring H1047R mutation in exon 20. Among the patients who undergo a curative resection of colorectal cancer, PIK3CA mutation is present in an important percentage of KRAS and BRAF wild type tumours. PIK3CA mutation may be considered as it could be a hypothetic reason to be not responder to anti-EGFR antibodies.

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Year:  2010        PMID: 20571907     DOI: 10.1007/s11033-010-0236-6

Source DB:  PubMed          Journal:  Mol Biol Rep        ISSN: 0301-4851            Impact factor:   2.316


  32 in total

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Review 4.  Hyperactive Ras in developmental disorders and cancer.

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5.  KRAS mutation status is predictive of response to cetuximab therapy in colorectal cancer.

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6.  PI3KCA/PTEN deregulation contributes to impaired responses to cetuximab in metastatic colorectal cancer patients.

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8.  Wild-type KRAS is required for panitumumab efficacy in patients with metastatic colorectal cancer.

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9.  Prevalence and heterogeneity of KRAS, BRAF, and PIK3CA mutations in primary colorectal adenocarcinomas and their corresponding metastases.

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  7 in total

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2.  The Prognostic Influence of BRAF Mutation and other Molecular, Clinical and Laboratory Parameters in Stage IV Colorectal Cancer.

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3.  PI3K expression and PIK3CA mutations are related to colorectal cancer metastases.

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4.  The Impact of Cetuximab Plus AKT- or mTOR- Inhibitor in a Patient-Derived Colon Cancer Cell Model with Wild-Type RAS and PIK3CA Mutation.

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5.  Mutation-Associated Phenotypic Heterogeneity in Novel and Canonical PIK3CA Helical and Kinase Domain Mutants.

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6.  PIK3CA activating mutation in colorectal carcinoma: associations with molecular features and survival.

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Review 7.  Current approaches for predicting a lack of response to anti-EGFR therapy in KRAS wild-type patients.

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  7 in total

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