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FAM83A is a potential biomarker for breast cancer initiation

BACKGROUND: Family with sequence similarity 83 member A (FAM83A) presents oncogenic properties in several cancers including breast cancer. Recently, we reported FAM83A overexpression in normal breast tissues from women at high risk of breast cancer. We now hypothesize that FAM83A is a key factor in...

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Autores principales: Marino, Natascia, German, Rana, Podicheti, Ram, Rockey, Pam, Sandusky, George E., Temm, Constance J., Nakshatri, Harikrishna, Addison, Rebekah J., Selman, Bryce, Althouse, Sandra K., Storniolo, Anna Maria V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8858535/
https://www.ncbi.nlm.nih.gov/pubmed/35183258
http://dx.doi.org/10.1186/s40364-022-00353-9
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author Marino, Natascia
German, Rana
Podicheti, Ram
Rockey, Pam
Sandusky, George E.
Temm, Constance J.
Nakshatri, Harikrishna
Addison, Rebekah J.
Selman, Bryce
Althouse, Sandra K.
Storniolo, Anna Maria V.
author_facet Marino, Natascia
German, Rana
Podicheti, Ram
Rockey, Pam
Sandusky, George E.
Temm, Constance J.
Nakshatri, Harikrishna
Addison, Rebekah J.
Selman, Bryce
Althouse, Sandra K.
Storniolo, Anna Maria V.
author_sort Marino, Natascia
collection PubMed
description BACKGROUND: Family with sequence similarity 83 member A (FAM83A) presents oncogenic properties in several cancers including breast cancer. Recently, we reported FAM83A overexpression in normal breast tissues from women at high risk of breast cancer. We now hypothesize that FAM83A is a key factor in breast cancer initiation. METHODS: Immunohistochemical staining was used to evaluate FAM83A protein levels in both a normal breast tissue microarray (TMA, N = 411) and a breast tumor TMA (N = 349). EGFR staining and its correlation with FAM83A expression were also assessed. Lentivirus-mediated manipulation of FAM83A expression in primary and hTERT-immortalized breast epithelial cells was employed. Biological and molecular alterations upon FAM83A overexpression/downregulation and FAM83A’s interaction partners were investigated. RESULTS: TMA analysis revealed a 1.5-fold increase in FAM83A expression level in breast cancer cases as compared with normal breast tissues (p < 0.0001). FAM83A protein expression was directly correlated with EGFR level in both normal and breast cancer tissues. In in vitro assays, exogenous expression of FAM83A in either primary or immortalized breast epithelial cells promoted cell viability and proliferation. Additionally, Ingenuity Pathway Analysis (IPA) revealed that FAM83A overexpression in primary cells affected the expression of genes involved in cellular morphology and metabolism. Mass spectrometry analysis identified DDX3X and LAMB3 as potential FAM83A interaction partners in primary cells, while we detected FAM83A interaction with cytoskeleton reorganization factors, including LIMA1, MYH10, PLEC, MYL6 in the immortalized cells. CONCLUSIONS: This study shows that FAM83A promotes metabolic activation in primary breast epithelial cells and cell proliferation in both primary and immortalized cells. These findings support its role in early breast oncogenesis. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40364-022-00353-9.
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spelling pubmed-88585352022-02-23 FAM83A is a potential biomarker for breast cancer initiation Marino, Natascia German, Rana Podicheti, Ram Rockey, Pam Sandusky, George E. Temm, Constance J. Nakshatri, Harikrishna Addison, Rebekah J. Selman, Bryce Althouse, Sandra K. Storniolo, Anna Maria V. Biomark Res Research BACKGROUND: Family with sequence similarity 83 member A (FAM83A) presents oncogenic properties in several cancers including breast cancer. Recently, we reported FAM83A overexpression in normal breast tissues from women at high risk of breast cancer. We now hypothesize that FAM83A is a key factor in breast cancer initiation. METHODS: Immunohistochemical staining was used to evaluate FAM83A protein levels in both a normal breast tissue microarray (TMA, N = 411) and a breast tumor TMA (N = 349). EGFR staining and its correlation with FAM83A expression were also assessed. Lentivirus-mediated manipulation of FAM83A expression in primary and hTERT-immortalized breast epithelial cells was employed. Biological and molecular alterations upon FAM83A overexpression/downregulation and FAM83A’s interaction partners were investigated. RESULTS: TMA analysis revealed a 1.5-fold increase in FAM83A expression level in breast cancer cases as compared with normal breast tissues (p < 0.0001). FAM83A protein expression was directly correlated with EGFR level in both normal and breast cancer tissues. In in vitro assays, exogenous expression of FAM83A in either primary or immortalized breast epithelial cells promoted cell viability and proliferation. Additionally, Ingenuity Pathway Analysis (IPA) revealed that FAM83A overexpression in primary cells affected the expression of genes involved in cellular morphology and metabolism. Mass spectrometry analysis identified DDX3X and LAMB3 as potential FAM83A interaction partners in primary cells, while we detected FAM83A interaction with cytoskeleton reorganization factors, including LIMA1, MYH10, PLEC, MYL6 in the immortalized cells. CONCLUSIONS: This study shows that FAM83A promotes metabolic activation in primary breast epithelial cells and cell proliferation in both primary and immortalized cells. These findings support its role in early breast oncogenesis. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40364-022-00353-9. BioMed Central 2022-02-19 /pmc/articles/PMC8858535/ /pubmed/35183258 http://dx.doi.org/10.1186/s40364-022-00353-9 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Marino, Natascia
German, Rana
Podicheti, Ram
Rockey, Pam
Sandusky, George E.
Temm, Constance J.
Nakshatri, Harikrishna
Addison, Rebekah J.
Selman, Bryce
Althouse, Sandra K.
Storniolo, Anna Maria V.
FAM83A is a potential biomarker for breast cancer initiation
title FAM83A is a potential biomarker for breast cancer initiation
title_full FAM83A is a potential biomarker for breast cancer initiation
title_fullStr FAM83A is a potential biomarker for breast cancer initiation
title_full_unstemmed FAM83A is a potential biomarker for breast cancer initiation
title_short FAM83A is a potential biomarker for breast cancer initiation
title_sort fam83a is a potential biomarker for breast cancer initiation
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8858535/
https://www.ncbi.nlm.nih.gov/pubmed/35183258
http://dx.doi.org/10.1186/s40364-022-00353-9
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