4.6 Review

Molecular subtyping of colorectal cancer: Recent progress, new challenges and emerging opportunities

期刊

SEMINARS IN CANCER BIOLOGY
卷 55, 期 -, 页码 37-52

出版社

ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD
DOI: 10.1016/j.semcancer.2018.05.002

关键词

Colorectal cancer; Heterogeneity; Molecular subtyping; Personalized medicine

类别

资金

  1. Research Grants Council of the Hong Kong Special Administrative Region, China [CityU 21101115]
  2. Science Technology and Innovation Committee of Shenzhen Municipality [JCYJ20170307091256048]
  3. National Cancer Institute, National Institute of Health [CA72851, CA181572, CA184792, CA187956, CA202797]
  4. Cancer Prevention Research Institute of Texas [RP140784]
  5. Sammons Cancer Center
  6. Baylor Foundation
  7. Baylor Scott & White Research Institute, Dallas, TX, USA
  8. City University of Hong Kong [7200455]
  9. VPRT from the City University of Hong Kong [9610337]

向作者/读者索取更多资源

Colorectal cancer (CRC) is one of the leading causes of cancer-related deaths worldwide. Similar to many other malignancies, CRC is a heterogeneous disease, making it a clinical challenge for optimization of treatment modalities in reducing the morbidity and mortality associated with this disease. A more precise understanding of the biological properties that distinguish patients with colorectal tumors, especially in terms of their clinical features, is a key requirement towards a more robust, targeted-drug design, and implementation of individualized therapies. In the recent decades, extensive studies have reported distinct CRC subtypes, with a mutation-centered view of tumor heterogeneity. However, more recently, the paradigm has shifted towards transcriptome-based classifications, represented by six independent CRC taxonomies. In 2015, the colorectal cancer subtyping consortium reported the identification of four consensus molecular subtypes (CMSs), providing thus far the most robust classification system for CRC. In this review, we summarize the historical timeline of CRC classification approaches; discuss their salient features and potential limitations that may require further refinement in near future. In other words, in spite of the recent encouraging progress, several major challenges prevent translation of molecular knowledge gleaned from CMSs into the clinic. Herein, we summarize some of these potential challenges and discuss exciting new opportunities currently emerging in related fields. We believe, close collaborations between basic researchers, bioinformaticians and clinicians are imperative for addressing these challenges, and eventually paving the path for CRC subtyping into routine clinical practice as we usher into the era of personalized medicine.

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