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Parity associates with chromosomal damage in uterine leiomyomas.
Kuisma, Heli; Bramante, Simona; Rajamäki, Kristiina; Sipilä, Lauri J; Kaasinen, Eevi; Kaukomaa, Jaana; Palin, Kimmo; Mäkinen, Netta; Sjöberg, Jari; Sarvilinna, Nanna; Taipale, Jussi; Kauppi, Liisa; Tumiati, Manuela; Hassinen, Antti; Pitkäniemi, Janne; Jalkanen, Jyrki; Heikkinen, Sanna; Pasanen, Annukka; Heikinheimo, Oskari; Bützow, Ralf; Välimäki, Niko; Aaltonen, Lauri A.
Affiliation
  • Kuisma H; Department of Medical and Clinical Genetics and Applied Tumor Genomics Research Program University of Helsinki, Helsinki, Finland.
  • Bramante S; Department of Medical and Clinical Genetics and Applied Tumor Genomics Research Program University of Helsinki, Helsinki, Finland.
  • Rajamäki K; Department of Medical and Clinical Genetics and Applied Tumor Genomics Research Program University of Helsinki, Helsinki, Finland.
  • Sipilä LJ; Department of Medical and Clinical Genetics and Applied Tumor Genomics Research Program University of Helsinki, Helsinki, Finland.
  • Kaasinen E; Department of Medical and Clinical Genetics and Applied Tumor Genomics Research Program University of Helsinki, Helsinki, Finland.
  • Kaukomaa J; Department of Medical and Clinical Genetics and Applied Tumor Genomics Research Program University of Helsinki, Helsinki, Finland.
  • Palin K; Department of Medical and Clinical Genetics and Applied Tumor Genomics Research Program University of Helsinki, Helsinki, Finland.
  • Mäkinen N; Department of Medical and Clinical Genetics and Applied Tumor Genomics Research Program University of Helsinki, Helsinki, Finland.
  • Sjöberg J; Department of Obstetrics and Gynecology, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.
  • Sarvilinna N; Department of Obstetrics and Gynecology, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.
  • Taipale J; Systems Oncology Research Program, University of Helsinki, Helsinki, Finland.
  • Kauppi L; Department of Medical and Clinical Genetics and Applied Tumor Genomics Research Program University of Helsinki, Helsinki, Finland.
  • Tumiati M; Systems Oncology Research Program, University of Helsinki, Helsinki, Finland.
  • Hassinen A; Systems Oncology Research Program, University of Helsinki, Helsinki, Finland.
  • Pitkäniemi J; FIMM-HCA, Institute for Molecular Medicine Finland (FIMM), Helsinki, Finland.
  • Jalkanen J; Institute for Statistical and Epidemiological Cancer Research, Finnish Cancer Registry, Helsinki, Finland.
  • Heikkinen S; Faculty of Social Sciences, University of Tampere, Tampere, Finland.
  • Pasanen A; Department of Public Health, University of Helsinki, Helsinki, Finland.
  • Heikinheimo O; Department of Obstetrics and Gynecology, Central Finland Central Hospital, Jyväskylä, Finland.
  • Bützow R; Institute for Statistical and Epidemiological Cancer Research, Finnish Cancer Registry, Helsinki, Finland.
  • Välimäki N; Department of Pathology, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.
  • Aaltonen LA; Department of Obstetrics and Gynecology, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.
Nat Commun ; 12(1): 5448, 2021 09 14.
Article in En | MEDLINE | ID: mdl-34521855
ABSTRACT
Mechanical forces in a constrained cellular environment were recently established as a facilitator of chromosomal damage. Whether this could contribute to tumorigenesis is not known. Uterine leiomyomas are common neoplasms that display relatively few chromosomal aberrations. We hypothesized that if mechanical forces contribute to chromosomal damage, signs of this could be seen in uterine leiomyomas from parous women. We examined the karyotypes of 1946 tumors, and found a striking overrepresentation of chromosomal damage associated with parity. We then subjected myometrial cells to physiological forces similar to those encountered during pregnancy, and found this to cause DNA breaks and a DNA repair response. While mechanical forces acting in constrained cellular environments may thus contribute to neoplastic degeneration, and genesis of uterine leiomyoma, further studies are needed to prove possible causality of the observed association. No evidence for progression to malignancy was found.
Subject(s)

Full text: 1 Database: MEDLINE Main subject: Parity / Uterine Neoplasms / Chromosome Aberrations / DNA Repair / Mediator Complex / Leiomyoma Type of study: Etiology_studies / Observational_studies / Risk_factors_studies Limits: Adult / Female / Humans / Pregnancy Language: En Journal: Nat Commun Journal subject: BIOLOGIA / CIENCIA Year: 2021 Type: Article Affiliation country: Finland

Full text: 1 Database: MEDLINE Main subject: Parity / Uterine Neoplasms / Chromosome Aberrations / DNA Repair / Mediator Complex / Leiomyoma Type of study: Etiology_studies / Observational_studies / Risk_factors_studies Limits: Adult / Female / Humans / Pregnancy Language: En Journal: Nat Commun Journal subject: BIOLOGIA / CIENCIA Year: 2021 Type: Article Affiliation country: Finland