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The Price of Human Evolution: Cancer-Testis Antigens, the Decline in Male Fertility and the Increase in Cancer

The increasing frequency of general and particularly male cancer coupled with the reduction in male fertility seen worldwide motivated us to seek a potential evolutionary link between these two phenomena, concerning the reproductive transcriptional modules observed in cancer and the expression of ca...

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Autores principales: Erenpreisa, Jekaterina, Vainshelbaum, Ninel Miriam, Lazovska, Marija, Karklins, Roberts, Salmina, Kristine, Zayakin, Pawel, Rumnieks, Felikss, Inashkina, Inna, Pjanova, Dace, Erenpreiss, Juris
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10380301/
https://www.ncbi.nlm.nih.gov/pubmed/37511419
http://dx.doi.org/10.3390/ijms241411660
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author Erenpreisa, Jekaterina
Vainshelbaum, Ninel Miriam
Lazovska, Marija
Karklins, Roberts
Salmina, Kristine
Zayakin, Pawel
Rumnieks, Felikss
Inashkina, Inna
Pjanova, Dace
Erenpreiss, Juris
author_facet Erenpreisa, Jekaterina
Vainshelbaum, Ninel Miriam
Lazovska, Marija
Karklins, Roberts
Salmina, Kristine
Zayakin, Pawel
Rumnieks, Felikss
Inashkina, Inna
Pjanova, Dace
Erenpreiss, Juris
author_sort Erenpreisa, Jekaterina
collection PubMed
description The increasing frequency of general and particularly male cancer coupled with the reduction in male fertility seen worldwide motivated us to seek a potential evolutionary link between these two phenomena, concerning the reproductive transcriptional modules observed in cancer and the expression of cancer-testis antigens (CTA). The phylostratigraphy analysis of the human genome allowed us to link the early evolutionary origin of cancer via the reproductive life cycles of the unicellulars and early multicellulars, potentially driving soma-germ transition, female meiosis, and the parthenogenesis of polyploid giant cancer cells (PGCCs), with the expansion of the CTA multi-families, very late during their evolution. CTA adaptation was aided by retrovirus domestication in the unstable genomes of mammals, for protecting male fertility in stress conditions, particularly that of humans, as compensation for the energy consumption of a large complex brain which also exploited retrotransposition. We found that the early and late evolutionary branches of human cancer are united by the immunity-proto-placental network, which evolved in the Cambrian and shares stress regulators with the finely-tuned sex determination system. We further propose that social stress and endocrine disruption caused by environmental pollution with organic materials, which alter sex determination in male foetuses and further spermatogenesis in adults, bias the development of PGCC-parthenogenetic cancer by default.
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spelling pubmed-103803012023-07-29 The Price of Human Evolution: Cancer-Testis Antigens, the Decline in Male Fertility and the Increase in Cancer Erenpreisa, Jekaterina Vainshelbaum, Ninel Miriam Lazovska, Marija Karklins, Roberts Salmina, Kristine Zayakin, Pawel Rumnieks, Felikss Inashkina, Inna Pjanova, Dace Erenpreiss, Juris Int J Mol Sci Review The increasing frequency of general and particularly male cancer coupled with the reduction in male fertility seen worldwide motivated us to seek a potential evolutionary link between these two phenomena, concerning the reproductive transcriptional modules observed in cancer and the expression of cancer-testis antigens (CTA). The phylostratigraphy analysis of the human genome allowed us to link the early evolutionary origin of cancer via the reproductive life cycles of the unicellulars and early multicellulars, potentially driving soma-germ transition, female meiosis, and the parthenogenesis of polyploid giant cancer cells (PGCCs), with the expansion of the CTA multi-families, very late during their evolution. CTA adaptation was aided by retrovirus domestication in the unstable genomes of mammals, for protecting male fertility in stress conditions, particularly that of humans, as compensation for the energy consumption of a large complex brain which also exploited retrotransposition. We found that the early and late evolutionary branches of human cancer are united by the immunity-proto-placental network, which evolved in the Cambrian and shares stress regulators with the finely-tuned sex determination system. We further propose that social stress and endocrine disruption caused by environmental pollution with organic materials, which alter sex determination in male foetuses and further spermatogenesis in adults, bias the development of PGCC-parthenogenetic cancer by default. MDPI 2023-07-19 /pmc/articles/PMC10380301/ /pubmed/37511419 http://dx.doi.org/10.3390/ijms241411660 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Erenpreisa, Jekaterina
Vainshelbaum, Ninel Miriam
Lazovska, Marija
Karklins, Roberts
Salmina, Kristine
Zayakin, Pawel
Rumnieks, Felikss
Inashkina, Inna
Pjanova, Dace
Erenpreiss, Juris
The Price of Human Evolution: Cancer-Testis Antigens, the Decline in Male Fertility and the Increase in Cancer
title The Price of Human Evolution: Cancer-Testis Antigens, the Decline in Male Fertility and the Increase in Cancer
title_full The Price of Human Evolution: Cancer-Testis Antigens, the Decline in Male Fertility and the Increase in Cancer
title_fullStr The Price of Human Evolution: Cancer-Testis Antigens, the Decline in Male Fertility and the Increase in Cancer
title_full_unstemmed The Price of Human Evolution: Cancer-Testis Antigens, the Decline in Male Fertility and the Increase in Cancer
title_short The Price of Human Evolution: Cancer-Testis Antigens, the Decline in Male Fertility and the Increase in Cancer
title_sort price of human evolution: cancer-testis antigens, the decline in male fertility and the increase in cancer
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10380301/
https://www.ncbi.nlm.nih.gov/pubmed/37511419
http://dx.doi.org/10.3390/ijms241411660
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