Unknown

Dataset Information

0

Mechanisms Behind the Resistance to Trastuzumab in HER2-Amplified Breast Cancer and Strategies to Overcome It.


ABSTRACT: The introduction of trastuzumab therapy markedly improved the poor prognosis associated with HER2-amplified breast cancers. Despite this, the presence of primary and acquired resistance to trastuzumab treatment remains a significant common challenge. The identification of resistance mechanisms and the incorporation of new drugs that achieve a better blockade of HER family receptors signaling have resulted in improved outcomes. The phosphatidylinositol 3'-kinase/protein kinase B/mammalian target of rapamycin pathway, cross-talk with estrogen receptors, immune response, cell cycle control mechanisms, and other tyrosine kinase receptors such as insulin-like growth factor I receptor are potential pathways involved in trastuzumab resistance. Different therapeutic interventions targeting these pathways are currently under evaluation.

SUBMITTER: Luque-Cabal M 

PROVIDER: S-EPMC4811269 | biostudies-literature | 2016

REPOSITORIES: biostudies-literature

altmetric image

Publications

Mechanisms Behind the Resistance to Trastuzumab in HER2-Amplified Breast Cancer and Strategies to Overcome It.

Luque-Cabal María M   García-Teijido Paula P   Fernández-Pérez Yolanda Y   Sánchez-Lorenzo Luisa L   Palacio-Vázquez Isabel I  

Clinical Medicine Insights. Oncology 20160328 Suppl 1


The introduction of trastuzumab therapy markedly improved the poor prognosis associated with HER2-amplified breast cancers. Despite this, the presence of primary and acquired resistance to trastuzumab treatment remains a significant common challenge. The identification of resistance mechanisms and the incorporation of new drugs that achieve a better blockade of HER family receptors signaling have resulted in improved outcomes. The phosphatidylinositol 3'-kinase/protein kinase B/mammalian target  ...[more]

Similar Datasets

| S-EPMC3858548 | biostudies-literature
| S-EPMC3357513 | biostudies-literature
| S-EPMC4261073 | biostudies-literature
| S-EPMC3536899 | biostudies-literature
| S-EPMC10439209 | biostudies-literature
| S-EPMC4243818 | biostudies-literature
2024-01-26 | PXD045804 | Pride
| S-EPMC6626398 | biostudies-literature
| S-EPMC7054312 | biostudies-literature
| S-EPMC9584623 | biostudies-literature