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Male origin microchimerism and brain cancer: a case-cohort study
Mads Kamper-Jørgensen1, Marianne Antonius Jakobsen2, Anne Tjønneland3,4
1Department of Public Health, Section of Epidemiology, University of Copenhagen, Øster Farimagsgade 5, Post Box 2099, 1014, Copenhagen K, Denmark. maka@sund.ku.dk.
Journal of Cancer Research and Clinical Oncology
|December 3, 2022
Summary
Women with male microchimerism, fetal cells persisting after pregnancy, had half the risk of brain cancer. This suggests pregnancy may protect against brain cancer by transferring fetal cells.
Area of Science:
- Oncology
- Immunology
- Reproductive Biology
Background:
- The etiology of brain cancer remains largely unknown.
- Pregnancy is associated with a reduced risk of brain cancer in women.
- Fetal microchimerism, the presence of fetal cells in the mother, is a potential mechanism linking pregnancy to cancer risk reduction.
Purpose of the Study:
- To investigate the association between male microchimerism and brain cancer risk in women.
- To determine if fetal cells persisting in women after pregnancy influence brain cancer development.
Main Methods:
- A case-cohort study design was employed.
- 73 women with brain cancer and 505 controls were analyzed.
- Male microchimerism was detected by Y chromosome sequences in blood samples.
Main Results:
- Women with male microchimerism had a 50% reduced risk of brain cancer compared to those without (Hazard Ratio = 0.50).
- Sensitivity analyses confirmed the robustness of the findings, ruling out bias or chance.
- This is the first study to demonstrate a link between male microchimerism and reduced brain cancer risk.
Conclusions:
- Male microchimerism is associated with a significantly lower risk of developing brain cancer in women.
- These findings support a protective role for pregnancy, potentially mediated by fetal cell transfer.
- The results align with previous research on microchimerism and other female cancers.

