Literature DB >> 30073926

Genetic Molecular Subtypes in Optimizing Personalized Therapy for Metastatic Colorectal Cancer.

Marcin Włodarczyk1,2, Jakub Włodarczyk1, Paweł Siwiński2, Aleksandra Sobolewska-Włodarczyk1,3, Jakub Fichna1.   

Abstract

Colorectal cancer (CRC) is a heterogeneous disease entity in terms of both molecular carcinogenesis and morphologic carcinogenesis multistep pathways. Considerable heterogeneity exists within CRC due to the varied genetic and epigenetic mechanisms involved in different carcinogenesis pathways. A better understanding of pathophysiology of tumors is necessary to develop modern and successful means of treatment in metastatic CRC. Over the last 5 years, there has been a surge in interest in the molecular classification of colorectal cancer, as its clinical importance both for predicting prognosis and in guiding personalized treatment had been acknowledged. Recently, the Colorectal Cancer Subtyping Consortium identified four consensus molecular subtypes, CMS 1-4 in CRC; however, attempts to stratify CRC using molecular features for prognostic and predictive purposes in clinical conditions had limited success. In this review, we focused on molecularly defined subtypes of CRC including specific mutations and discuss implications for current and future patient management in metastatic CRC to achieve the maximal therapeutic response for each patient, while reducing adverse side effects of therapy. Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.org.

Entities:  

Keywords:  Consensus molecular subtypes; carcinogenesis; chemotherapy; chromosomal instability; colorectal cancer; microsatellitezzm321990instability.

Mesh:

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Year:  2018        PMID: 30073926     DOI: 10.2174/1389450119666180803122744

Source DB:  PubMed          Journal:  Curr Drug Targets        ISSN: 1389-4501            Impact factor:   3.465


  7 in total

Review 1.  Back to the Colorectal Cancer Consensus Molecular Subtype Future.

Authors:  David G Menter; Jennifer S Davis; Bradley M Broom; Michael J Overman; Jeffrey Morris; Scott Kopetz
Journal:  Curr Gastroenterol Rep       Date:  2019-01-30

2.  MiR-137-3p Inhibits Colorectal Cancer Cell Migration by Regulating a KDM1A-Dependent Epithelial-Mesenchymal Transition.

Authors:  Xiaoling Ding; Jie Zhang; Ziqin Feng; Qianru Tang; Xiaorong Zhou
Journal:  Dig Dis Sci       Date:  2020-08-04       Impact factor: 3.199

3.  Detection of Human papillomavirus and the role of p16INK4a in colorectal carcinomas.

Authors:  Larisse Silva Dalla Libera; Thalita de Siqueira; Igor Lopes Santos; Jéssica Enocencio Porto Ramos; Amanda Xavier Milhomen; Rita de Cassia Gonçalves de Alencar; Silvia Helena Rabelo Santos; Megmar Aparecida Dos Santos Carneiro; Rosane Ribeiro Figueiredo Alves; Vera Aparecida Saddi
Journal:  PLoS One       Date:  2020-06-25       Impact factor: 3.240

4.  Triple blockade of EGFR, MEK and PD-L1 has antitumor activity in colorectal cancer models with constitutive activation of MAPK signaling and PD-L1 overexpression.

Authors:  S Napolitano; N Matrone; A L Muddassir; G Martini; A Sorokin; V De Falco; E F Giunta; D Ciardiello; E Martinelli; V Belli; M Furia; S Kopetz; F Morgillo; F Ciardiello; T Troiani
Journal:  J Exp Clin Cancer Res       Date:  2019-12-16

Review 5.  Consensus molecular subtypes of colorectal cancer in clinical practice: A translational approach.

Authors:  Guillermo Valenzuela; Joaquín Canepa; Carolina Simonetti; Loreto Solo de Zaldívar; Katherine Marcelain; Jaime González-Montero
Journal:  World J Clin Oncol       Date:  2021-11-24

6.  Implications of Intratumor Heterogeneity on Consensus Molecular Subtype (CMS) in Colorectal Cancer.

Authors:  Saikat Chowdhury; Matan Hofree; Kangyu Lin; Dipen Maru; Scott Kopetz; John Paul Shen
Journal:  Cancers (Basel)       Date:  2021-09-30       Impact factor: 6.639

7.  S-Adenosylmethionine Treatment of Colorectal Cancer Cell Lines Alters DNA Methylation, DNA Repair and Tumor Progression-Related Gene Expression.

Authors:  Sára Zsigrai; Alexandra Kalmár; Zsófia B Nagy; Barbara K Barták; Gábor Valcz; Krisztina A Szigeti; Orsolya Galamb; Titanilla Dankó; Anna Sebestyén; Gábor Barna; Vanessza Szabó; Orsolya Pipek; Anna Medgyes-Horváth; István Csabai; Zsolt Tulassay; Péter Igaz; István Takács; Béla Molnár
Journal:  Cells       Date:  2020-08-09       Impact factor: 6.600

  7 in total

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