Evidence map›Paper›PMID 32772147›Full record

ArticleWorld journal of urology2021

Reduced cytoplasmic expression of MAGE-A2 predicts tumor aggressiveness and survival: an immunohistochemical analysis.

Azadeh Khalvandi, Maryam Abolhasani, Zahra Madjd, Laleh Sharifi, Parisa Bakhshi, Monireh Mohsenzadegan

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Article in World journal of urology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.2field-weighted citation impact, top 47% of its field
1 · What the graph read from it

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3 · Its place in the literature

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4 citing papers in PubMed, 6 citations in OpenAlex.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors at 2 institutions in 1 country.

Azadeh KhalvandiDepartment of Immunology, School of Medicine, Iran University of Medical Sciences, Tehran, Iran.
Maryam AbolhasaniHasheminejad Kidney Center, Iran University of Medical Sciences, Tehran, Iran.
Zahra MadjdOncopathology Research Center, Iran University of Medical Sciences, Tehran, Iran.
Laleh SharifiUro-Oncology Research Center, Tehran University of Medical Sciences, Tehran, Iran.
Parisa BakhshiDepartment of Medical Biotechnology, Faculty of Allied Medical Sciences, Iran University of Medical Sciences, Tehran, Iran.
Monireh MohsenzadeganDepartment of Medical Laboratory Sciences, Faculty of Allied Medical Sciences, Iran University of Medical Sciences (IUMS), Hemmat Highway, Tehran, Iran. monirehmohsenzadegan@gmail.com.ORCID http://orcid.org/0000-0003-2434-9728
Iran University of Medical Sciences · IRTehran University of Medical Sciences · IR

Funding

Iran University of Medical Sciences 31-33720
6 · The paper itself

Abstract

backgroundMelanoma antigen gene A2 (MAGE-A2) is one of the most cancer-testis antigens overexpressed in various types of cancers. Silencing the MAGE-A2 expression inhibited the proliferation of prostate cancer (PCa) cells and increased the chemosensitivity. However, the expression pattern of MAGE-A2 in PCa tissue samples and its prognostic and therapeutic values for PCa patients is still unclear.

methodsIn this study, for the first time, the staining pattern and clinical significance of MAGE-A2 were evaluated in 166 paraffin-embedded prostate tissues, including 148 cases of PCa and 18 cases of high-grade prostatic intraepithelial neoplasia (HPIN), by immunohistochemical analysis.

resultsThe simultaneous expression of both nuclear and cytoplasmic patterns of MAGE-A2 with different staining intensities was observed among studied cases. Increased expression of MAGE-A2 was significantly found in PCa tissues compared to HPIN cases (P < 0.0001). Among PCa samples, the strong staining intensity of nuclear expression was predominantly observed in comparison with cytoplasmic expression in PCa tissues (P < 0.0001). A significant and inverse correlation was found between the cytoplasmic expression of MAGE-A2 and increased Gleason score (P = 0.002). Increased cytoplasmic expression of MAGE-A2 was associated with longer biochemical recurrence-free survival (BCR-FS) and disease-free survival (DFS) of patients (P = 0.002, P = 0.001, respectively). In multivariate analysis, Gleason score and cytoplasmic expression of MAGE-A2 were independent predictors of the BCR-FS (P = 0.014; P = 0.028, respectively).

conclusionsTaken together, cytoplasmic expression of MAGE-A2 was inversely proportional to the malignant grade and duration of recurrence of the disease in patients with PCa.

Indexed as

Gene Expression Regulation, NeoplasticAgedAged, 80 and overCytoplasmHumansImmunohistochemistryMaleMelanoma-Specific AntigensMiddle AgedNeoplasm ProteinsPrognosisProstatic NeoplasmsSurvival RateMageA2 protein, humanMelanoma-Specific AntigensNeoplasm ProteinsHigh-grade prostatic intraepithelial neoplasia (HPIN)ImmunohistochemistryMAGE-A2Prostate cancer (PCa)

Identifiers

PMID32772147
OpenAlexW3047955989

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.