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Identification of tumor antigens in malignant mesothelioma

Serological analysis of recombinant tumor cDNA expression library (SEREX) is a powerful and widely used method to explore the cancer immune environment. In the present study, immunoscreening of normal testicular tissues and malignant mesothelioma (MM) cancer MSTO-211H cell line cDNA libraries with s...

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Autores principales: Kim, Ye-Rin, Song, Myung-Ha, Lee, Jun-Won, Bae, Jae-Ho, Kim, Jong-Eun, Kang, Dong-Muk, Lee, Sang-Yull
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5649555/
https://www.ncbi.nlm.nih.gov/pubmed/29085453
http://dx.doi.org/10.3892/ol.2017.6805
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author Kim, Ye-Rin
Song, Myung-Ha
Lee, Jun-Won
Bae, Jae-Ho
Kim, Jong-Eun
Kang, Dong-Muk
Lee, Sang-Yull
author_facet Kim, Ye-Rin
Song, Myung-Ha
Lee, Jun-Won
Bae, Jae-Ho
Kim, Jong-Eun
Kang, Dong-Muk
Lee, Sang-Yull
author_sort Kim, Ye-Rin
collection PubMed
description Serological analysis of recombinant tumor cDNA expression library (SEREX) is a powerful and widely used method to explore the cancer immune environment. In the present study, immunoscreening of normal testicular tissues and malignant mesothelioma (MM) cancer MSTO-211H cell line cDNA libraries with sera from 5 MM patients led to the isolation of 16 independent antigens, which were designated ‘Korea Pusan-Malignant Mesothelioma’ (KP-MM)-1 to −16. In total, 3/16 antigens were identified using the results of previous SEREX analyses, and 13 were newly identified. Of these, KP-MM-8, which was subsequently identified as amyotrophic lateral sclerosis 2 chromosome region candidate 11, was shown to be tissue-restricted. Reverse transcription-polymerase chain reaction demonstrated KP-MM-8 to be expressed strongly only in the normal testis, and weakly in the spleen, prostate, ovary, heart and skeletal muscle. In addition, KP-MM-8 mRNA was identified in MM cell lines, and in various other cancer cell lines, including MM (3/4), lung cancer (5/7), melanoma (5/7) and liver cancer (5/5) cell lines. Additionally, 2/16 antigens (KP-MM-2 and KP-MM-6) exclusively reacted with sera from cancer patients. However, KP-MM-8 reacted with 1 of 8 MM sera. Notably, 8/8 patients with MM and 8/8 normal individuals exhibited antibodies reactive to KP-MM-5, which was identified as cell division cycle 25B, a known oncogene. Overall, this data suggests that KP-MM-8 may be considered as a cancer/testis-like antigen and KP-MM-5 as an immunogenic tumor antigen in MM patients.
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spelling pubmed-56495552017-10-30 Identification of tumor antigens in malignant mesothelioma Kim, Ye-Rin Song, Myung-Ha Lee, Jun-Won Bae, Jae-Ho Kim, Jong-Eun Kang, Dong-Muk Lee, Sang-Yull Oncol Lett Articles Serological analysis of recombinant tumor cDNA expression library (SEREX) is a powerful and widely used method to explore the cancer immune environment. In the present study, immunoscreening of normal testicular tissues and malignant mesothelioma (MM) cancer MSTO-211H cell line cDNA libraries with sera from 5 MM patients led to the isolation of 16 independent antigens, which were designated ‘Korea Pusan-Malignant Mesothelioma’ (KP-MM)-1 to −16. In total, 3/16 antigens were identified using the results of previous SEREX analyses, and 13 were newly identified. Of these, KP-MM-8, which was subsequently identified as amyotrophic lateral sclerosis 2 chromosome region candidate 11, was shown to be tissue-restricted. Reverse transcription-polymerase chain reaction demonstrated KP-MM-8 to be expressed strongly only in the normal testis, and weakly in the spleen, prostate, ovary, heart and skeletal muscle. In addition, KP-MM-8 mRNA was identified in MM cell lines, and in various other cancer cell lines, including MM (3/4), lung cancer (5/7), melanoma (5/7) and liver cancer (5/5) cell lines. Additionally, 2/16 antigens (KP-MM-2 and KP-MM-6) exclusively reacted with sera from cancer patients. However, KP-MM-8 reacted with 1 of 8 MM sera. Notably, 8/8 patients with MM and 8/8 normal individuals exhibited antibodies reactive to KP-MM-5, which was identified as cell division cycle 25B, a known oncogene. Overall, this data suggests that KP-MM-8 may be considered as a cancer/testis-like antigen and KP-MM-5 as an immunogenic tumor antigen in MM patients. D.A. Spandidos 2017-10 2017-08-24 /pmc/articles/PMC5649555/ /pubmed/29085453 http://dx.doi.org/10.3892/ol.2017.6805 Text en Copyright: © Kim et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
Kim, Ye-Rin
Song, Myung-Ha
Lee, Jun-Won
Bae, Jae-Ho
Kim, Jong-Eun
Kang, Dong-Muk
Lee, Sang-Yull
Identification of tumor antigens in malignant mesothelioma
title Identification of tumor antigens in malignant mesothelioma
title_full Identification of tumor antigens in malignant mesothelioma
title_fullStr Identification of tumor antigens in malignant mesothelioma
title_full_unstemmed Identification of tumor antigens in malignant mesothelioma
title_short Identification of tumor antigens in malignant mesothelioma
title_sort identification of tumor antigens in malignant mesothelioma
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5649555/
https://www.ncbi.nlm.nih.gov/pubmed/29085453
http://dx.doi.org/10.3892/ol.2017.6805
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