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Molecular subtyping of gastric cancer with respect to the growth pattern of lymph-node metastases

  • Original Article – Cancer Research
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Abstract

Purpose

Gastric cancer is the third leading cause of cancer-related death. Recently, innovative diagnostic and prognostic molecular subtypes have been proposed. We revealed that extranodal extension (ENE) of lymph-node metastases independently influences survival. Therefore, the aim of the present study was to evaluate novel molecular subtyping with regard to the growth pattern of lymph-node metastases.

Methods

A total of 189 gastric carcinomas with lymph-node metastases were analyzed. The expression of p53, SOX2, SOX9, and the mismatch-repair gene products MLH1, PMS2, MSH2, and MSH6 were analyzed by immunohistochemistry. To determine the correlation with EBV infection, in situ hybridization for EBV-encoded small RNA (EBER) was applied.

Results

ENE was present in 36% of patients. EBV-positive carcinoma was evident in 5.8%, and p53 aberrant (chromosomal instable) tumors in 22.2%, a gastric cancer with deficient mismatch-repair status in 9%, and MSS/p53neg/EBVneg tumors were seen in 63% of patients. There was no significant correlation between the presence or absence of ENE and the molecular subtypes. However, a significant association between molecular subgroups and the Lauren classification, the oncogene SOX2, and tumor grading was detected.

Conclusion

The present findings suggest that alterations in gastric cancer leading to ENE are not associated with alterations underpinning the molecular subgroups. Nonetheless, molecular subtyping on the basis of IHC and ISH is feasible and might become clinical routine. Thus, further studies are needed to clarify the mechanisms of extranodal extension in gastric cancer.

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Abbreviations

95% CI:

95% Confidence intervals

ACRG:

Asian Cancer Research Group

CIN:

Chromosomal instability

dMMR:

Deficient mismatch repair

pMMR:

Proficient mismatch repair

EBER:

EBV-encoded small RNA

EBV:

Epstein–Barr virus

ENE:

Extranodal extension

FFPE:

Formalin-fixed and paraffin-embedded

GC:

Gastric cancer

ING:

Intranodal growth

IHC:

Immunohistochemistry

ISH:

In situ hybridization

MSI:

Microsatellite instability

TCGA:

The Cancer Genome Atlas

TMA:

Tissue microarray

WHO:

World health organization

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Authors

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Correspondence to Jens Neumann.

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Conflict of interest

The authors wish to confirm that there are no known conflicts of interest associated with this publication and there has been no significant financial support for this work that could have influenced its outcome.

Ethical approval

The study was carried out according to the recommendations of the local ethics committee of the Medical Faculty of the Ludwig-Maximilians-University Munich, Germany. This retrospective study was performed with irreversibly anonymized data sets and tissue specimens. Thus, ethical approval or written consent was not required. The study was performed according to the standards laid out in the declaration of Helsinki 1975. All researchers were blinded to the patient data during the experimental analysis.

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Bösch, F., Todorova, R., Link, H. et al. Molecular subtyping of gastric cancer with respect to the growth pattern of lymph-node metastases. J Cancer Res Clin Oncol 145, 2689–2697 (2019). https://doi.org/10.1007/s00432-019-03029-4

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  • DOI: https://doi.org/10.1007/s00432-019-03029-4

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