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Genetic Mutations and Epigenetic Modifications: Driving Cancer and Informing Precision Medicine

期刊

BIOMED RESEARCH INTERNATIONAL
卷 2017, 期 -, 页码 -

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HINDAWI LTD
DOI: 10.1155/2017/9620870

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资金

  1. Canadian Institutes of Health Research (CIHR) [MOP-130304]
  2. CIHR
  3. DalhousieMedical Research Foundation (DMRF)
  4. Beatrice Hunter Cancer Research Institute (BHCRI)
  5. Canadian Imperial Bank of Commerce as part of the Terry Fox Strategic Health Research Training Program in Cancer Research at CIHR
  6. Banting Research Foundation and the BHCRI

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Cancer treatment is undergoing a significant revolution from one-size-fits-all cytotoxic therapies to tailored approaches that precisely target molecular alterations. Precision strategies for drug development and patient stratification, based on the molecular features of tumors, are the next logical step in a long history of approaches to cancer therapy. In this review, we discuss the history of cancer treatment from generic natural extracts and radical surgical procedures to site-specific and combinatorial treatment regimens, which have incrementally improved patient outcomes. We discuss the related contributions of genetics and epigenetics to cancer progression and the response to targeted therapies and identify challenges and opportunities for the success of precision medicine. The identification of patients who will benefit from targeted therapies is more complex than simply identifying patients whose tumors harbour the targeted aberration, and intratumoral heterogeneity makes it difficult to determine if a precision therapy is successful during treatment. This heterogeneity enables tumors to develop resistance to targeted approaches; therefore, the rational combination of therapeutic agents will limit the threat of acquired resistance to therapeutic success. By incorporating the view of malignant transformation modulated by networks of genetic and epigenetic interactions, molecular strategies will enable precision medicine for effective treatment across cancer subtypes.

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