Sex reporting of cells used in cancer research: A systematic review.
Mi-Na ParkSung-Eun KimSungin ChoiYoomee ChangHyeyoon KimHa-Eun LeeSuk Kyeong LeeMi-Kyung SungHee Young PaikPublished in: FASEB journal : official publication of the Federation of American Societies for Experimental Biology (2024)
Sex and gender disparities in biomedical research have been emphasized to improve scientific knowledge applied for the health of both men and women. Despite sex differences in cancer incidence, prognosis, and responses to therapeutic agents, mechanistic explanations at molecular levels are far from enough. Recent studies suggested that cell sex is an important biological variable due to differences in sex chromosome gene expression and differences in events associated with developmental biology. The objective of this study was to analyze the reporting of sex of cells used in cancer research using articles published in Cancer Cell, Molecular Cancer, Journal of Hematology & Oncology, Journal for ImmunoTherapy of Cancer, and Cancer Research in 2020, and to examine whether there exists any sex bias. We found that the percentage of cells with sex notation in the article was 36.5%. Primary cells exhibited higher sex notation compared to cell lines. A higher percentage of female cells were used in cell cultures with sex notation. Also, sex-common cells omitted sex description more often compared to sex-specific cells. None of the cells isolated from embryo and esophagus reported the cell sex in the article. Our results indicate cell sex report in cancer research is limited to a small proportion of cells used in the study. These results call for acknowledging the sex of cells to increase the applicability of biomedical research discoveries.
Keyphrases
- induced apoptosis
- cell cycle arrest
- gene expression
- healthcare
- squamous cell
- endoplasmic reticulum stress
- randomized controlled trial
- oxidative stress
- emergency department
- squamous cell carcinoma
- stem cells
- risk assessment
- dna methylation
- cell proliferation
- copy number
- palliative care
- pi k akt
- genome wide
- childhood cancer