Literature DB >> 25120768

Overexpression of MAGE-D4 in colorectal cancer is a potentially prognostic biomarker and immunotherapy target.

Qing-Mei Zhang1, Shu-Jia He1, Ning Shen2, Bin Luo1, Rong Fan1, Jun Fu1, Guo-Rong Luo1, Su-Fang Zhou1, Shao-Wen Xiao3, Xiao-Xun Xie1.   

Abstract

Melanoma-associated antigen D4 (MAGE-D4) is a novel member of MAGE family. This study aimed to examine the expression and immunogenicity of MAGE-D4 in colorectal cancer (CRC) to determine its potential as a prognosis and immunotherapeutic target. The expression of MAGE-D4 mRNA and protein was determined by RT-PCR and immunohistochemistry (IHC) in CRCs with paired adjacent non-tumor tissues, colorectal adenomas and normal colorectal tissues, respectively. Sera from 64 CRC patients were tested for MAGE-D4 antibody by ELISA. MAGE-D4 mRNA was more frequently expressed in CRCs (76.7%, 46/60) than in adjacent non-tumor tissues (15.0%, 9/60). MAGE-D4 protein was detected in all the CRC tissues tested, 70.0% of which showed high expression. There was no MAGE-D4 protein detected in any paired adjacent non-tumor tissue. No MAGE-D4 expression was found in colorectal adenomas and normal colorectal tissues by either RT-PCR or immunohistochemistry. Patients with high MAGE-D4 protein expression had significantly shorter overall survival than those with low MAGE-D4 protein expression (median, 68.6 vs 122.2 months; P=0.030). Furthermore, multivariate analysis exhibited high MAGE-D4 protein expression had a trend toward an independent prognostic factor (hazard ratio: 6.124; P=0.050). Humoral immunity to MAGE-D4 was detected in 12 of 64 (18.8%) CRC patients' sera but not in 77 healthy donors. There was no correlation between MAGE-D4 expression, serum antibody and clinicopathological parameters. These findings suggest MAGE-D4 may serve as a potentially prognostic biomarker and an attractive target of immunotherapy in CRC.

Entities:  

Keywords:  MAGE-D4; Melanoma-associated antigen; colorectal cancer; serum immunoreactivity

Mesh:

Substances:

Year:  2014        PMID: 25120768      PMCID: PMC4129003     

Source DB:  PubMed          Journal:  Int J Clin Exp Pathol        ISSN: 1936-2625


  45 in total

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Authors:  J H Bond
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Authors:  Richard A Morgan; Nachimuthu Chinnasamy; Daniel Abate-Daga; Alena Gros; Paul F Robbins; Zhili Zheng; Mark E Dudley; Steven A Feldman; James C Yang; Richard M Sherry; Giao Q Phan; Marybeth S Hughes; Udai S Kammula; Akemi D Miller; Crystal J Hessman; Ashley A Stewart; Nicholas P Restifo; Martha M Quezado; Meghna Alimchandani; Avi Z Rosenberg; Avindra Nath; Tongguang Wang; Bibiana Bielekova; Simone C Wuest; Nirmala Akula; Francis J McMahon; Susanne Wilde; Barbara Mosetter; Dolores J Schendel; Carolyn M Laurencot; Steven A Rosenberg
Journal:  J Immunother       Date:  2013-02       Impact factor: 4.456

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Review 1.  Novel cancer antigens for personalized immunotherapies: latest evidence and clinical potential.

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Journal:  Ther Adv Med Oncol       Date:  2016-01       Impact factor: 8.168

Review 2.  Immunotherapy in human colorectal cancer: Challenges and prospective.

Authors:  Xuan Sun; Jian Suo; Jun Yan
Journal:  World J Gastroenterol       Date:  2016-07-28       Impact factor: 5.742

3.  Expression profile of ACTL8, CTCFL, OIP5 and XAGE3 in glioma and their prognostic significance: a retrospective clinical study.

Authors:  Xisheng Li; Lidong Ning; Qingmei Zhang; Yingying Ge; Chang Liu; Shuiqing Bi; Xia Zeng; Weixia Nong; Song Wu; Gaoshui Guo; Shaowen Xiao; Bin Luo; Xiaoxun Xie
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4.  Identification of a seven-gene signature predicting clinical outcome of liver cancer based on tumor mutational burden.

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5.  High expression of MAGE-C1 gene in colorectal cancer is associated with its poor prognosis.

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6.  FMR1NB Involved in Glioma Tumorigenesis Is a Promising Target for Prognosis and Therapy.

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7.  MAGED4B Promotes Glioma Progression via Inactivation of the TNF-α-induced Apoptotic Pathway by Down-regulating TRIM27 Expression.

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Review 8.  Colorectal Cancer Immunotherapy: Options and Strategies.

Authors:  Nor Adzimah Johdi; Nur Fazilah Sukor
Journal:  Front Immunol       Date:  2020-09-18       Impact factor: 7.561

9.  Combined treatment with epigenetic agents enhances anti-tumor activity of MAGE-D4 peptide-specific T cells by upregulating the MAGE-D4 expression in glioma.

Authors:  Shui-Qing Bi; Qing-Mei Zhang; Xia Zeng; Chang Liu; Wei-Xia Nong; Huan Xie; Feng Li; Li-Na Lin; Bin Luo; Ying-Ying Ge; Xiao-Xun Xie
Journal:  Front Oncol       Date:  2022-08-03       Impact factor: 5.738

10.  Prognostic and clinicopathological value of melanoma-associated antigen D4 in patients with glioma.

Authors:  Jun Yan; Jing Wen; Zong-Dang Wei; Xi-Sheng Li; Ping Li; Shao-Wen Xiao
Journal:  Oncol Lett       Date:  2018-01-26       Impact factor: 2.967

  10 in total

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