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The debatable presence of PIWI‐interacting RNAs in invasive breast cancer

Numerous factors influence breast cancer (BC) prognosis, thus complicating the prediction of outcome. By identifying biomarkers that would distinguish the cases with poorer response to therapy already at the time of diagnosis, the rate of survival could be improved. Lately, Piwi‐interacting RNAs (pi...

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Autores principales: Kärkkäinen, Emmi, Heikkinen, Sami, Tengström, Maria, Kosma, Veli‐Matti, Mannermaa, Arto, Hartikainen, Jaana M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8178507/
https://www.ncbi.nlm.nih.gov/pubmed/33960684
http://dx.doi.org/10.1002/cam4.3915
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author Kärkkäinen, Emmi
Heikkinen, Sami
Tengström, Maria
Kosma, Veli‐Matti
Mannermaa, Arto
Hartikainen, Jaana M.
author_facet Kärkkäinen, Emmi
Heikkinen, Sami
Tengström, Maria
Kosma, Veli‐Matti
Mannermaa, Arto
Hartikainen, Jaana M.
author_sort Kärkkäinen, Emmi
collection PubMed
description Numerous factors influence breast cancer (BC) prognosis, thus complicating the prediction of outcome. By identifying biomarkers that would distinguish the cases with poorer response to therapy already at the time of diagnosis, the rate of survival could be improved. Lately, Piwi‐interacting RNAs (piRNAs) have been introduced as potential cancer biomarkers, however, due to the recently raised challenges in piRNA annotations, further evaluation of piRNAs’ involvement in cancer is required. We performed small RNA sequencing in 227 fresh‐frozen breast tissue samples from the Eastern Finnish Kuopio Breast Cancer Project material to study the presence of piRNAs in BC and their associations with the clinicopathological features and outcome of BC patients. We observed the presence of three small RNAs annotated as piRNA database entries (DQ596932, DQ570994, and DQ571955) in our samples. The actual species of these RNAs however remain uncertain. All three small RNAs were upregulated in grade III tumors and DQ596932 additionally in estrogen receptor negative tumors. Furthermore, patients with estrogen receptor positive BC and higher DQ571955 had shorter relapse‐free survival and poorer BC‐specific survival, thus indicating DQ571955 as a candidate predictive marker for radiotherapy response in estrogen receptor positive BC. DQ596932 showed possible prognostic value in BC, whereas DQ570994 was identified as a candidate predictive marker for tamoxifen and chemotherapy response. These three small RNAs appear as candidate biomarkers for BC, which could after further investigation provide novel approaches for the treatment of therapy resistant BC. Overall, our results indicate that the prevalence of piRNAs in cancer is most likely not as comprehensive as has been previously thought.
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spelling pubmed-81785072021-06-15 The debatable presence of PIWI‐interacting RNAs in invasive breast cancer Kärkkäinen, Emmi Heikkinen, Sami Tengström, Maria Kosma, Veli‐Matti Mannermaa, Arto Hartikainen, Jaana M. Cancer Med Clinical Cancer Research Numerous factors influence breast cancer (BC) prognosis, thus complicating the prediction of outcome. By identifying biomarkers that would distinguish the cases with poorer response to therapy already at the time of diagnosis, the rate of survival could be improved. Lately, Piwi‐interacting RNAs (piRNAs) have been introduced as potential cancer biomarkers, however, due to the recently raised challenges in piRNA annotations, further evaluation of piRNAs’ involvement in cancer is required. We performed small RNA sequencing in 227 fresh‐frozen breast tissue samples from the Eastern Finnish Kuopio Breast Cancer Project material to study the presence of piRNAs in BC and their associations with the clinicopathological features and outcome of BC patients. We observed the presence of three small RNAs annotated as piRNA database entries (DQ596932, DQ570994, and DQ571955) in our samples. The actual species of these RNAs however remain uncertain. All three small RNAs were upregulated in grade III tumors and DQ596932 additionally in estrogen receptor negative tumors. Furthermore, patients with estrogen receptor positive BC and higher DQ571955 had shorter relapse‐free survival and poorer BC‐specific survival, thus indicating DQ571955 as a candidate predictive marker for radiotherapy response in estrogen receptor positive BC. DQ596932 showed possible prognostic value in BC, whereas DQ570994 was identified as a candidate predictive marker for tamoxifen and chemotherapy response. These three small RNAs appear as candidate biomarkers for BC, which could after further investigation provide novel approaches for the treatment of therapy resistant BC. Overall, our results indicate that the prevalence of piRNAs in cancer is most likely not as comprehensive as has been previously thought. John Wiley and Sons Inc. 2021-05-07 /pmc/articles/PMC8178507/ /pubmed/33960684 http://dx.doi.org/10.1002/cam4.3915 Text en © 2021 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Cancer Research
Kärkkäinen, Emmi
Heikkinen, Sami
Tengström, Maria
Kosma, Veli‐Matti
Mannermaa, Arto
Hartikainen, Jaana M.
The debatable presence of PIWI‐interacting RNAs in invasive breast cancer
title The debatable presence of PIWI‐interacting RNAs in invasive breast cancer
title_full The debatable presence of PIWI‐interacting RNAs in invasive breast cancer
title_fullStr The debatable presence of PIWI‐interacting RNAs in invasive breast cancer
title_full_unstemmed The debatable presence of PIWI‐interacting RNAs in invasive breast cancer
title_short The debatable presence of PIWI‐interacting RNAs in invasive breast cancer
title_sort debatable presence of piwi‐interacting rnas in invasive breast cancer
topic Clinical Cancer Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8178507/
https://www.ncbi.nlm.nih.gov/pubmed/33960684
http://dx.doi.org/10.1002/cam4.3915
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