Interferon/STAT1 and neuregulin signaling pathways are exploratory biomarkers of cetuximab (Erbitux®) efficacy in KRAS wild-type squamous carcinomas: A pathway-based analysis of whole human-genome microarray data from cetuximab-adapted tumor cell-line models

  • Authors:
    • Cristina Oliveras-Ferraros
    • Alejandro Vazquez-Martin
    • Bernardo Queralt
    • Manuel Adrados
    • Rosa Ortiz
    • Silvia Cufí
    • Xavier Hernández-Yagüe
    • Raquel Guardeño
    • Luciana Báez
    • Begoña Martin-Castillo
    • Maria Carmen Pérez-Martínez
    • Eugeni Lopez-Bonet
    • Rafael De Llorens
    • Luis Bernadó
    • Joan Brunet
    • Javier A. Menendez
  • View Affiliations

  • Published online on: August 9, 2011     https://doi.org/10.3892/ijo.2011.1155
  • Pages: 1455-1479
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Abstract

KRAS mutation status is being used as the sole biomarker to predict therapeutic efficacy of cetuximab in metastatic colorectal cancer (mCRC). A significant number of mCRC patients with KRAS wild-type (WT) tumors, however, do not benefit from cetuximab. We are also lacking efficacy predictors in head and neck squamous cell carcinomas with an intact KRAS signaling and in non-small cell lung cancer in which KRAS mutations do not predict cetuximab efficacy. We recently established pre-clinical models of EGFR gene-amplified KRAS WT A431 squamous carcinoma cells chronically adapted to grow in the presence of cetuximab. We employed the ingenuity pathway analysis software to functionally interpret data from Agilent's whole human genome arrays in the context of biological processes, networks, and pathways. Cetuximab-induced activation of the interferon (IFN)/STAT1 appeared to switch from ‘growth inhibitory’ in acutely-treated cells to ‘pro-survival’ in chronically-adapted cells. Cetuximab treatment appeared to negatively select initially dominant IFN-sensitive clones and promoted selection of IFN- and cetuximab-refractory tumor clones constitutively bearing an up-regulated IFN/STAT1 signaling. High-levels of mRNAs coding for the EGFR ligands amphiregulin (AREG), epiregulin (EREG), and neuregulin-1/heregulin (NRG1) predicted for acute cetuximab's functioning. Chronic cetuximab, however, appeared to negatively select initially dominant AREG/EREG/NRG1-positive clones to promote selection of cetuximab-refractory clones exhibiting a knocked-down neuregulin signaling. Our current evolutionary mapping of the transcriptomic changes that occur during cetuximab-induced chronic blockade of EGFR/KRAS WT signaling strongly suggests that mRNAs coding for IFN/STAT1- and EGFR ligands-related genes can be evaluated as novel predictors of efficacy in KRAS WT squamous cancer patients being treated with cetuximab.

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December 2011
Volume 39 Issue 6

Print ISSN: 1019-6439
Online ISSN:1791-2423

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Spandidos Publications style
Oliveras-Ferraros C, Vazquez-Martin A, Queralt B, Adrados M, Ortiz R, Cufí S, Hernández-Yagüe X, Guardeño R, Báez L, Martin-Castillo B, Martin-Castillo B, et al: Interferon/STAT1 and neuregulin signaling pathways are exploratory biomarkers of cetuximab (Erbitux®) efficacy in KRAS wild-type squamous carcinomas: A pathway-based analysis of whole human-genome microarray data from cetuximab-adapted tumor cell-line models. Int J Oncol 39: 1455-1479, 2011.
APA
Oliveras-Ferraros, C., Vazquez-Martin, A., Queralt, B., Adrados, M., Ortiz, R., Cufí, S. ... Menendez, J.A. (2011). Interferon/STAT1 and neuregulin signaling pathways are exploratory biomarkers of cetuximab (Erbitux®) efficacy in KRAS wild-type squamous carcinomas: A pathway-based analysis of whole human-genome microarray data from cetuximab-adapted tumor cell-line models. International Journal of Oncology, 39, 1455-1479. https://doi.org/10.3892/ijo.2011.1155
MLA
Oliveras-Ferraros, C., Vazquez-Martin, A., Queralt, B., Adrados, M., Ortiz, R., Cufí, S., Hernández-Yagüe, X., Guardeño, R., Báez, L., Martin-Castillo, B., Pérez-Martínez, M. ., Lopez-Bonet, E., De Llorens, R., Bernadó, L., Brunet, J., Menendez, J. A."Interferon/STAT1 and neuregulin signaling pathways are exploratory biomarkers of cetuximab (Erbitux®) efficacy in KRAS wild-type squamous carcinomas: A pathway-based analysis of whole human-genome microarray data from cetuximab-adapted tumor cell-line models". International Journal of Oncology 39.6 (2011): 1455-1479.
Chicago
Oliveras-Ferraros, C., Vazquez-Martin, A., Queralt, B., Adrados, M., Ortiz, R., Cufí, S., Hernández-Yagüe, X., Guardeño, R., Báez, L., Martin-Castillo, B., Pérez-Martínez, M. ., Lopez-Bonet, E., De Llorens, R., Bernadó, L., Brunet, J., Menendez, J. A."Interferon/STAT1 and neuregulin signaling pathways are exploratory biomarkers of cetuximab (Erbitux®) efficacy in KRAS wild-type squamous carcinomas: A pathway-based analysis of whole human-genome microarray data from cetuximab-adapted tumor cell-line models". International Journal of Oncology 39, no. 6 (2011): 1455-1479. https://doi.org/10.3892/ijo.2011.1155