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NanoString expression profiling identifies candidate biomarkers of RAD001 response in metastatic gastric cancer.

Publication ,  Journal Article
Das, K; Chan, XB; Epstein, D; Te Teh, B; Kim, K-M; Kim, ST; Park, SH; Kang, WK; Rozen, S; Lee, J; Tan, P
Published in: ESMO Open
2016

BACKGROUND: Gene expression profiling has contributed greatly to cancer research. However, expression-driven biomarker discovery in metastatic gastric cancer (mGC) remains unclear. A gene expression profile predicting RAD001 response in refractory GC was explored in this study. METHODS: Total RNA isolated from 54 tumour specimens from patients with mGC, prior to RAD001 treatment, was analysed via the NanoString nCounter gene expression assay. This assay targeted 477 genes representing 10 different GC-related oncogenic signalling and molecular subtype-specific expression signatures. Gene expression profiles were correlated with patient clinicopathological variables. RESULTS: NanoString data confirmed similar gene expression profiles previously identified by microarray analysis. Signature I with 3 GC subtypes (mesenchymal, metabolic and proliferative) showed approximately 90% concordance where the mesenchymal and proliferative subtypes were significantly associated with signet ring cell carcinoma and the WHO classified tubular adenocarcinoma GC, respectively (p=0.042). Single-gene-level correlations with patient clinicopathological variables showed strong associations between FHL1 expression (mesenchymal subtype) and signet ring cell carcinoma, and NEK2, OIP5, PRC1, TPX2 expression (proliferative subtype) with tubular adenocarcinoma (adjusted p<0.05). Increased BRCA2 (p=0.040) and MMP9 (p=0.045) expression was significantly associated with RAD001 good response and longer progression-free survival outcome (BRCA2, p=0.012, HR 0.370 95% CI (0.171 to 0.800); MMP9, p=0.010, HR 0.359 95% CI (0.166 to 0.779)). In contrast, increased BTC (p=0.035) expression was significantly associated with RAD001 poor response and poor progression-free survival (p=0.031, HR 2.336 95% CI (1.079 to 5.059) by univariate Cox regression analysis. CONCLUSIONS: Microarray results are highly reproducible with NanoString nCounter gene expression profiling. Additionally, BRCA2 and MMP9 expression are potential predictive biomarkers for good response in RAD001-treated mGC.

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Published In

ESMO Open

DOI

ISSN

2059-7029

Publication Date

2016

Volume

1

Issue

1

Start / End Page

e000009

Location

England

Related Subject Headings

  • 3211 Oncology and carcinogenesis
 

Citation

APA
Chicago
ICMJE
MLA
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Das, K., Chan, X. B., Epstein, D., Te Teh, B., Kim, K.-M., Kim, S. T., … Tan, P. (2016). NanoString expression profiling identifies candidate biomarkers of RAD001 response in metastatic gastric cancer. ESMO Open, 1(1), e000009. https://doi.org/10.1136/esmoopen-2015-000009
Das, Kakoli, Xiu Bin Chan, David Epstein, Binan Te Teh, Kyoung-Mee Kim, Seung Tae Kim, Se Hoon Park, et al. “NanoString expression profiling identifies candidate biomarkers of RAD001 response in metastatic gastric cancer.ESMO Open 1, no. 1 (2016): e000009. https://doi.org/10.1136/esmoopen-2015-000009.
Das K, Chan XB, Epstein D, Te Teh B, Kim K-M, Kim ST, et al. NanoString expression profiling identifies candidate biomarkers of RAD001 response in metastatic gastric cancer. ESMO Open. 2016;1(1):e000009.
Das, Kakoli, et al. “NanoString expression profiling identifies candidate biomarkers of RAD001 response in metastatic gastric cancer.ESMO Open, vol. 1, no. 1, 2016, p. e000009. Pubmed, doi:10.1136/esmoopen-2015-000009.
Das K, Chan XB, Epstein D, Te Teh B, Kim K-M, Kim ST, Park SH, Kang WK, Rozen S, Lee J, Tan P. NanoString expression profiling identifies candidate biomarkers of RAD001 response in metastatic gastric cancer. ESMO Open. 2016;1(1):e000009.

Published In

ESMO Open

DOI

ISSN

2059-7029

Publication Date

2016

Volume

1

Issue

1

Start / End Page

e000009

Location

England

Related Subject Headings

  • 3211 Oncology and carcinogenesis