Literature DB >> 30631039

CD44v6 engages in colorectal cancer progression.

Lixin Ma1, Lihua Dong2, Pengyu Chang3.   

Abstract

CD44 is a transmembrane glycoprotein. When the CD44 gene is expressed, its pre-messenger RNA (mRNA) can be alternatively spliced into mature mRNAs that encode several CD44 isoforms. The mRNA assembles with ten standard exons, and the sixth variant exon encodes CD44v6, which engages in a variety of biological processes, including cell growth, apoptosis, migration, and angiogenesis. Mechanistically, CD44v6 interacts with hyaluronic acid (HA) or osteopontin, or it acts as a coreceptor for various cytokines, such as epidermal growth factor, vascular endothelial growth factor, hepatocyte growth factor, and C-X-C motif chemokine 12. In this context, the receptor tyrosine kinase or G protein-coupled receptor-associated signaling pathways, including mitogen-activated protein kinase/extracellular-signal-regulated kinase and phosphoinositide-3-kinase/Akt, are activated. Using these actions, homeostasis or regeneration can be facilitated among normal tissues. However, overexpression of the mature mRNA encoding CD44v6 can induce cancer progression. For example, CD44v6 assists colorectal cancer stem cells in colonization, invasion, and metastasis. Overexpression of CD44v6 predicts poor prognosis in patients with colorectal cancer, as patients with a large number of CD44v6-positive cells in their tumors are generally diagnosed at late stages. Thus, the clinical significance of CD44v6 in colorectal cancer deserves consideration. Preclinical results have indicated satisfactory efficacies of anti-CD44 therapy among several cancers, including prostate cancer, pancreatic cancer, and gastric cancer. Moreover, clinical trials aiming to evaluate the pharmacokinetics, pharmacodynamics, efficacy, and toxicity of a commercialized anti-CD44 monoclonal antibody developed by Roche (RO5429083) have been conducted among patients with CD44-expressing malignant tumors, and a clinical trial focusing on the dose escalation of this antibody is ongoing. Thus, we are hopeful that anti-CD44 therapy will be applied in the treatment of colorectal cancer in the future.

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Year:  2019        PMID: 30631039      PMCID: PMC6328617          DOI: 10.1038/s41419-018-1265-7

Source DB:  PubMed          Journal:  Cell Death Dis            Impact factor:   8.469


  37 in total

Review 1.  CD44-Targeted Nanocarrier for Cancer Therapy.

Authors:  Prashant Kesharwani; Rahul Chadar; Afsana Sheikh; Waleed Y Rizg; Awaji Y Safhi
Journal:  Front Pharmacol       Date:  2022-03-31       Impact factor: 5.810

Review 2.  Role of CD44 isoforms in epithelial-mesenchymal plasticity and metastasis.

Authors:  Mark Primeaux; Saiprasad Gowrikumar; Punita Dhawan
Journal:  Clin Exp Metastasis       Date:  2022-01-12       Impact factor: 5.150

3.  Identification of Circular RNA-Based Immunomodulatory Networks in Colorectal Cancer.

Authors:  Zongfeng Feng; Leyan Li; Yi Tu; Xufeng Shu; Yang Zhang; Qingwen Zeng; Lianghua Luo; Ahao Wu; Wenzheng Chen; Yi Cao; Zhengrong Li
Journal:  Front Oncol       Date:  2022-01-27       Impact factor: 6.244

4.  Role of endoplasmic reticulum stress in apoptosis induced by HK2 inhibitor and its potential as a new drug combination strategy.

Authors:  Jiateng Zhong; Shuya Lu; Xiaoling Jia; Qian Li; Lei Liu; Pei Xie; Guodong Wang; Manman Lu; Wuji Gao; Tiesuo Zhao; Qianqing Wang; Wei Su; Na Li
Journal:  Cell Stress Chaperones       Date:  2022-03-30       Impact factor: 3.827

5.  Altered Expression of MBNL Family of Alternative Splicing Factors in Colorectal Cancer.

Authors:  Nazila Navvabi; Pavla Kolikova; Petr Hosek; Frantisek Zitricky; Azita Navvabi; Ondrej Vycital; Jan Bruha; Richard Palek; Jachym Rosendorf; Vaclav Liska; Pavel Pitule
Journal:  Cancer Genomics Proteomics       Date:  2021 May-Jun       Impact factor: 4.069

6.  Cancer-associated fibroblasts secrete hypoxia-induced serglycin to promote head and neck squamous cell carcinoma tumor cell growth in vitro and in vivo by activating the Wnt/β-catenin pathway.

Authors:  Junqi Xie; Xiaofeng Qi; Yufeng Wang; Xiteng Yin; Wenguang Xu; Shengwei Han; Yu Cai; Wei Han
Journal:  Cell Oncol (Dordr)       Date:  2021-03-02       Impact factor: 6.730

7.  A novel tumor suppressor role of myosin light chain kinase splice variants through downregulation of the TEAD4/CD44 axis.

Authors:  Yen-Ju Huang; Tsung-Chun Lee; Yu-Chen Pai; Been-Ren Lin; Jerrold R Turner; Linda Chia-Hui Yu
Journal:  Carcinogenesis       Date:  2021-07-16       Impact factor: 4.944

8.  The Interaction between Reactive Peritoneal Mesothelial Cells and Tumor Cells via Extracellular Vesicles Facilitates Colorectal Cancer Dissemination.

Authors:  Simona Serratì; Letizia Porcelli; Francesco Fragassi; Marianna Garofoli; Roberta Di Fonte; Livia Fucci; Rosa Maria Iacobazzi; Antonio Palazzo; Francesca Margheri; Grazia Cristiani; Anna Albano; Raffaele De Luca; Donato Francesco Altomare; Michele Simone; Amalia Azzariti
Journal:  Cancers (Basel)       Date:  2021-05-20       Impact factor: 6.639

Review 9.  Beyond Colonoscopy: Exploring New Cell Surface Biomarkers for Detection of Early, Heterogenous Colorectal Lesions.

Authors:  Saleh Ramezani; Arianna Parkhideh; Pratip K Bhattacharya; Mary C Farach-Carson; Daniel A Harrington
Journal:  Front Oncol       Date:  2021-07-05       Impact factor: 6.244

10.  The correlation of epithelial-mesenchymal transition-related gene expression and the clinicopathologic features of colorectal cancer patients in Taiwan.

Authors:  Yuan-Chang Dai; Chuan-Yin Fang; Hsin-Yi Yang; Yi-Jun Jian; Shou-Chieh Wang; Yi-Wen Liu
Journal:  PLoS One       Date:  2021-07-02       Impact factor: 3.240

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