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原发性和转移性黑色素瘤中硫酸软骨素蛋白聚糖4蛋白的免疫组织化学检测

Immunohistochemical detection of the chondroitin sulfate proteoglycan 4 protein in primary and metastatic melanoma.

作者信息

Grossauer Anna, Uranowska Karolina, Kitzwögerer Melitta, Mostegel Margit, Breiteneder Heimo, Hafner Christine

机构信息

Department of Dermatology, University Hospital St. Poelten, Karl Landsteiner University of Health Sciences, A-3100 St. Poelten, Austria.

Department of Pathology, University Hospital Krems, Karl Landsteiner University of Health Sciences, A-3500 Krems an der Donau, Austria.

出版信息

Oncol Lett. 2023 Jul 20;26(3):382. doi: 10.3892/ol.2023.13968. eCollection 2023 Sep.

Abstract

Treatment of malignant melanoma, the most aggressive form of skin cancer, continues to be a major challenge for clinicians. New targeted therapies with kinase inhibitors or drugs which modify the immune response are often accompanied by the development of resistance or severe side effects. In this context, chondroitin sulfate proteoglycan 4 (CSPG4), a highly immunogenic melanoma tumor antigen, could be a potential target for alternative therapeutic approaches. The aim of the present study was to identify differences in the levels of CSPG4 protein expression in primary and metastatic melanomas as well as to analyze correlations between CSPG4 expression and histopathological data and patient characteristics. A total of 189 melanoma tissue samples from Lower Austria, including primary melanomas and melanoma metastases, were immunohistochemically stained for the expression of CSPG4 and statistical analyses were performed. A total of 65.6% of melanoma tissue samples stained positive for the expression of CSPG4. Primary nodular and primary superficial spreading melanomas demonstrated a significantly higher number of positively stained tissue samples for CSPG4 compared with primary lentigo maligna melanomas. No significant differences in the expression of CSPG4 were demonstrated between primary melanomas and melanoma metastases. The present study supports the advancement of the understanding of CSPG4 tissue expression patterns in melanoma patients and provides additional information for further investigation of CSPG4 as a potential therapeutic target.

摘要

恶性黑色素瘤是皮肤癌中最具侵袭性的一种,其治疗仍然是临床医生面临的一项重大挑战。激酶抑制剂或调节免疫反应的新型靶向疗法往往伴随着耐药性的产生或严重的副作用。在这种背景下,硫酸软骨素蛋白聚糖4(CSPG4)是一种高度免疫原性的黑色素瘤肿瘤抗原,可能是替代治疗方法的潜在靶点。本研究的目的是确定原发性和转移性黑色素瘤中CSPG4蛋白表达水平的差异,并分析CSPG4表达与组织病理学数据及患者特征之间的相关性。对来自下奥地利州的189份黑色素瘤组织样本(包括原发性黑色素瘤和黑色素瘤转移灶)进行CSPG4表达的免疫组化染色,并进行统计分析。共有65.6%的黑色素瘤组织样本CSPG4表达呈阳性。与原发性恶性雀斑样痣黑色素瘤相比,原发性结节性和原发性浅表扩散性黑色素瘤中CSPG4阳性染色的组织样本数量显著更多。原发性黑色素瘤和黑色素瘤转移灶之间CSPG4的表达未显示出显著差异。本研究有助于加深对黑色素瘤患者CSPG4组织表达模式的理解,并为进一步研究CSPG4作为潜在治疗靶点提供更多信息。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e9f3/10407859/65c854b5ac0d/ol-26-03-13968-g00.jpg

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