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NanoString expression profiling identifies candidate biomarkers of RAD001 response in metastatic gastric cancer
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 is...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5070203/ https://www.ncbi.nlm.nih.gov/pubmed/27843583 http://dx.doi.org/10.1136/esmoopen-2015-000009 |
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author | Das, Kakoli Chan, Xiu Bin Epstein, David Teh, Bin Tean Kim, Kyoung-Mee Kim, Seung Tae Park, Se Hoon Kang, Won Ki Rozen, Steve Lee, Jeeyun Tan, Patrick |
author_facet | Das, Kakoli Chan, Xiu Bin Epstein, David Teh, Bin Tean Kim, Kyoung-Mee Kim, Seung Tae Park, Se Hoon Kang, Won Ki Rozen, Steve Lee, Jeeyun Tan, Patrick |
author_sort | Das, Kakoli |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-5070203 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-50702032016-11-14 NanoString expression profiling identifies candidate biomarkers of RAD001 response in metastatic gastric cancer Das, Kakoli Chan, Xiu Bin Epstein, David Teh, Bin Tean Kim, Kyoung-Mee Kim, Seung Tae Park, Se Hoon Kang, Won Ki Rozen, Steve Lee, Jeeyun Tan, Patrick ESMO Open Original Article 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. BMJ Publishing Group 2016-02-17 /pmc/articles/PMC5070203/ /pubmed/27843583 http://dx.doi.org/10.1136/esmoopen-2015-000009 Text en Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing/ This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ |
spellingShingle | Original Article Das, Kakoli Chan, Xiu Bin Epstein, David Teh, Bin Tean Kim, Kyoung-Mee Kim, Seung Tae Park, Se Hoon Kang, Won Ki Rozen, Steve Lee, Jeeyun Tan, Patrick NanoString expression profiling identifies candidate biomarkers of RAD001 response in metastatic gastric cancer |
title | NanoString expression profiling identifies candidate biomarkers of RAD001 response in metastatic gastric cancer |
title_full | NanoString expression profiling identifies candidate biomarkers of RAD001 response in metastatic gastric cancer |
title_fullStr | NanoString expression profiling identifies candidate biomarkers of RAD001 response in metastatic gastric cancer |
title_full_unstemmed | NanoString expression profiling identifies candidate biomarkers of RAD001 response in metastatic gastric cancer |
title_short | NanoString expression profiling identifies candidate biomarkers of RAD001 response in metastatic gastric cancer |
title_sort | nanostring expression profiling identifies candidate biomarkers of rad001 response in metastatic gastric cancer |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5070203/ https://www.ncbi.nlm.nih.gov/pubmed/27843583 http://dx.doi.org/10.1136/esmoopen-2015-000009 |
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