TRANSCRIPTIONAL PROFILE OF CANCER-TESTICULAR ANTIGENS IN PATIENTS WITH BREAST CANCER

To identify new effective targets for immunotherapy of breast cancer, based on cancer-testis antigens (CTA), the associations were studied between CTA gene expression, clinical and pathological characteristics of breast cancer. Therefore, the aim of the study was to perform screening of CTAs specifi...

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Autores principales: D. I. Vodolazhskiy, D. S. Kutilin, Kh. A. Mogushkova, O. I. Kit
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Lenguaje:RU
Publicado: SPb RAACI 2018
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Acceso en línea:https://doaj.org/article/88cf9366e4b0431181328b35e86d63c2
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spelling oai:doaj.org-article:88cf9366e4b0431181328b35e86d63c22021-11-18T08:03:47ZTRANSCRIPTIONAL PROFILE OF CANCER-TESTICULAR ANTIGENS IN PATIENTS WITH BREAST CANCER1563-06252313-741X10.15789/1563-0625-2018-3-383-390https://doaj.org/article/88cf9366e4b0431181328b35e86d63c22018-06-01T00:00:00Zhttps://www.mimmun.ru/mimmun/article/view/1542https://doaj.org/toc/1563-0625https://doaj.org/toc/2313-741XTo identify new effective targets for immunotherapy of breast cancer, based on cancer-testis antigens (CTA), the associations were studied between CTA gene expression, clinical and pathological characteristics of breast cancer. Therefore, the aim of the study was to perform screening of CTAs specific to breast tissue tumors (luminal types A and B) based on assessment of the transcriptional profile of cancer-testis genes in the patients of different ages. To evaluate these relations, paired surgical biopsies (normal and tumor) of breast tissue of 32 patients (64 samples) aged 38-86 years were used. Relative expression of 16 genetic loci (MAGEA1, MAGEA2, MAGEA3, MAGEA4, MAGEB1, MAGEB2, GAGE1, GAGE3, GAGE4, MAGEC1, BAGE, XAGE3, NY-ESO1, SSX2, SYCP1 and PRAME1) was determined by the RT-qPCR. It was found that the transcriptional profile of CTA differs in different age groups of patients (at the age of < 55 years, overexpression of MAGEA3 was noted; after 55 years, MAGEA1, MAGEB1, BAGE, NY-ESO1, GAGE1 and GAGE3 were more expressed). In the luminal type A cancer, overexpression of MAGEA1, MAGEA2, MAGEA4, MAGEB1, MAGEB2, GAGE3, GAGE4, MAGEC1 and PRAME1, whereas in B type cancer, the genes with increased expression were not detected. These differences should be considered when planning immunotherapy, can be used as biomarkers for both breast cancer as clinical entity, and, in particular, for its individual subtypes.D. I. VodolazhskiyD. S. KutilinKh. A. MogushkovaO. I. KitSPb RAACIarticlegene expressionreal-time qpcrcancer-testicular antigens (cta)breast cancerimmunotherapyImmunologic diseases. AllergyRC581-607RUMedicinskaâ Immunologiâ, Vol 20, Iss 3, Pp 383-390 (2018)
institution DOAJ
collection DOAJ
language RU
topic gene expression
real-time qpcr
cancer-testicular antigens (cta)
breast cancer
immunotherapy
Immunologic diseases. Allergy
RC581-607
spellingShingle gene expression
real-time qpcr
cancer-testicular antigens (cta)
breast cancer
immunotherapy
Immunologic diseases. Allergy
RC581-607
D. I. Vodolazhskiy
D. S. Kutilin
Kh. A. Mogushkova
O. I. Kit
TRANSCRIPTIONAL PROFILE OF CANCER-TESTICULAR ANTIGENS IN PATIENTS WITH BREAST CANCER
description To identify new effective targets for immunotherapy of breast cancer, based on cancer-testis antigens (CTA), the associations were studied between CTA gene expression, clinical and pathological characteristics of breast cancer. Therefore, the aim of the study was to perform screening of CTAs specific to breast tissue tumors (luminal types A and B) based on assessment of the transcriptional profile of cancer-testis genes in the patients of different ages. To evaluate these relations, paired surgical biopsies (normal and tumor) of breast tissue of 32 patients (64 samples) aged 38-86 years were used. Relative expression of 16 genetic loci (MAGEA1, MAGEA2, MAGEA3, MAGEA4, MAGEB1, MAGEB2, GAGE1, GAGE3, GAGE4, MAGEC1, BAGE, XAGE3, NY-ESO1, SSX2, SYCP1 and PRAME1) was determined by the RT-qPCR. It was found that the transcriptional profile of CTA differs in different age groups of patients (at the age of < 55 years, overexpression of MAGEA3 was noted; after 55 years, MAGEA1, MAGEB1, BAGE, NY-ESO1, GAGE1 and GAGE3 were more expressed). In the luminal type A cancer, overexpression of MAGEA1, MAGEA2, MAGEA4, MAGEB1, MAGEB2, GAGE3, GAGE4, MAGEC1 and PRAME1, whereas in B type cancer, the genes with increased expression were not detected. These differences should be considered when planning immunotherapy, can be used as biomarkers for both breast cancer as clinical entity, and, in particular, for its individual subtypes.
format article
author D. I. Vodolazhskiy
D. S. Kutilin
Kh. A. Mogushkova
O. I. Kit
author_facet D. I. Vodolazhskiy
D. S. Kutilin
Kh. A. Mogushkova
O. I. Kit
author_sort D. I. Vodolazhskiy
title TRANSCRIPTIONAL PROFILE OF CANCER-TESTICULAR ANTIGENS IN PATIENTS WITH BREAST CANCER
title_short TRANSCRIPTIONAL PROFILE OF CANCER-TESTICULAR ANTIGENS IN PATIENTS WITH BREAST CANCER
title_full TRANSCRIPTIONAL PROFILE OF CANCER-TESTICULAR ANTIGENS IN PATIENTS WITH BREAST CANCER
title_fullStr TRANSCRIPTIONAL PROFILE OF CANCER-TESTICULAR ANTIGENS IN PATIENTS WITH BREAST CANCER
title_full_unstemmed TRANSCRIPTIONAL PROFILE OF CANCER-TESTICULAR ANTIGENS IN PATIENTS WITH BREAST CANCER
title_sort transcriptional profile of cancer-testicular antigens in patients with breast cancer
publisher SPb RAACI
publishDate 2018
url https://doaj.org/article/88cf9366e4b0431181328b35e86d63c2
work_keys_str_mv AT divodolazhskiy transcriptionalprofileofcancertesticularantigensinpatientswithbreastcancer
AT dskutilin transcriptionalprofileofcancertesticularantigensinpatientswithbreastcancer
AT khamogushkova transcriptionalprofileofcancertesticularantigensinpatientswithbreastcancer
AT oikit transcriptionalprofileofcancertesticularantigensinpatientswithbreastcancer
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