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Epstein–Barr virus-associated gastric cancer reveals intratumoral heterogeneity of PIK3CA mutations

Böger, C. ; Krüger, S. ; Behrens, H.M. ; Bock, S. ; Haag, J. ; Kalthoff, H. ; Röcken, C.

Annals of oncology, 2017-05, Vol.28 (5), p.1005-1014 [Periódico revisado por pares]

England: Elsevier Ltd

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Título:
Epstein–Barr virus-associated gastric cancer reveals intratumoral heterogeneity of PIK3CA mutations
Autor: Böger, C. ; Krüger, S. ; Behrens, H.M. ; Bock, S. ; Haag, J. ; Kalthoff, H. ; Röcken, C.
Assuntos: Adenocarcinoma - genetics ; Adenocarcinoma - mortality ; Adenocarcinoma - secondary ; Adenocarcinoma - virology ; Aged ; biomarker ; Class I Phosphatidylinositol 3-Kinases - genetics ; EBV ; Epstein-Barr Virus Infections - genetics ; Epstein-Barr Virus Infections - mortality ; Epstein-Barr Virus Infections - pathology ; Epstein-Barr Virus Infections - virology ; Female ; Gene Frequency ; Genetic Association Studies ; Genetic Heterogeneity ; Genetic Predisposition to Disease ; High-Throughput Nucleotide Sequencing ; Humans ; intratumoral heterogeneity ; Kaplan-Meier Estimate ; lymph node metastases ; Lymphatic Metastasis ; Male ; Molecular Diagnostic Techniques ; Mutation ; next generation sequencing ; Original ; PI3K pathway ; Stomach Neoplasms - genetics ; Stomach Neoplasms - mortality ; Stomach Neoplasms - pathology ; Stomach Neoplasms - virology
É parte de: Annals of oncology, 2017-05, Vol.28 (5), p.1005-1014
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SourceType-Scholarly Journals-1
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Descrição: Recent whole-genome sequencing identified four molecular subtypes of gastric cancer (GC), of which the subgroup of Epstein–Barr virus-associated GC (EBVaGC) showed a significant enrichment of PIK3CA mutations. We here aimed to validate independently the enrichment of PIK3CA mutations in EBVaGC of a Central European GC cohort, to correlate EBV status with clinico-pathological patient characteristics and to test for a major issue of GC, intratumoral heterogeneity. In a first step, 484 GCs were screened for EBV and PIK3CA hot spot mutations of exon 9/20 using EBER in situ hybridization and pyrosequencing, respectively. Secondly, an extended sequencing of PIK3CA also utilizing next generation sequencing was carried out in all EBVaGCs and 96 corresponding lymph node metastases. Twenty-two GCs were EBER-positive, all being of latency type I. Intratumoral heterogeneity of EBER-positivity was found in 18% of EBVaGCs. Twenty-three GCs held PIK3CA mutations in hot spot regions of exon 9 or 20, being significantly more common in EBVaGCs (P<0.001). Subsequent extended sequencing of PIK3CA of EBVaGCs showed that 14% harvested three to five different PIK3CA genotypes (including wildtype) in the same primary tumor, albeit in histologically and spatially distinct tumor areas, and that intratumoral heterogeneity of PIK3CA was also present in the corresponding lymph node metastases. Our findings unravel issues of tumor heterogeneity and illustrate that the assessment of the EBV status in tissue biopsies might carry the risk of sampling errors, which may significantly hamper adequate molecular tumor classification in a more clinical setting. Moreover, this is the first report of intratumoral heterogeneity of PIK3CA mutations in GC, and our findings lead to the conclusion that PIK3CA mutant and -wildtype tumor subclones are skilled to metastasize independently to different regional lymph nodes.
Editor: England: Elsevier Ltd
Idioma: Inglês

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Epstein–Barr virus-associated gastric cancer reveals intratumoral heterogeneity of PIK3CA mutations

Böger, C. ; Krüger, S. ; Behrens, H.M. ; Bock, S. ; Haag, J. ; Kalthoff, H. ; Röcken, C.

England: Elsevier Ltd

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