- Characteristics of BAK1 serum levels in women with endometrial hyperplastic processes associated with obesity
Characteristics of BAK1 serum levels in women with endometrial hyperplastic processes associated with obesity
Ukrainian Journal Health of Woman. 2026. 3(184): 39-43. doi: 10.15574/HW.2026.3(184).3943
Marichereda V. G., Drobot D. I.
Odesa National Medical University, Ukraine
For citation: Marichereda VG, Drobot DI. (2026). Characteristics of BAK1 serum levels in women with endometrial hyperplastic processes associated with obesity. Ukrainian Journal Health of Woman. 3(184): 39-43. doi: 10.15574/HW.2026.3(184).3943
Article received: Apr 01, 2026. Accepted for publication: Jun 01, 2026.
Aim – to evaluate serum BAK1 levels in women with endometrial hyperplastic processes associated with obesity and to determine their diagnostic and prognostic significance.
Materials and methods. The study included 103 patients: group Ia – endometrial hyperplasia without atypia (n=39); group Ib – atypical hyperplasia (n=9); group II – endometrial cancer (n=25); group III – polyendocrine metabolic ovarian syndrome (PMOS, n=16); group IV – healthy women (n=14). The diagnosis was histologically verified. Body mass index (BMI) was calculated according to WHO criteria, serum BAK1 level was measured by ELISA, and all participants underwent transabdominal and transvaginal pelvic ultrasound.
Results. Body weight and BMI in groups Ia, Ib, and II were comparable and corresponded to obesity criteria, while lower values were observed in groups III and IV. BAK1 levels differed significantly between groups, exhibiting high variability. The lowest levels were observed in group Ib, suggesting suppressed apoptotic mechanisms during precancerous transformation; levels were moderately reduced in group II and highest in group IV, reflecting preserved apoptotic control. Ultrasound showed increased M-echo thickness, heterogeneous structure, and altered vascularization in groups Ia and II, whereas ovarian changes predominated in group III.
Conclusions. The findings confirm the clinical association of obesity and metabolic disorders with endometrial hyperplastic and neoplastic processes. BAK1 levels change depending on the degree of pathological transformation and are lowest in atypical hyperplasia, indicating impaired apoptotic regulation. The nonlinear relationship between BAK1 and endometrial thickness reflects the complexity of molecular control of proliferative processes. BAK1 may be considered as a promising biomarker of apoptosis impairment and a potential predictor of neoplastic transformation in women with metabolic disorders, which requires confirmation in larger cohorts.
The study was conducted in accordance with the principles of the Declaration of Helsinki. Written informed consent was obtained from all participating women.
The authors declare no conflict of interest.
Keywords: endometrium, hyperplasia, obesity, apoptosis, carcinoma, insulin resistance.
REFERENCES
1. Fine Biotech Co., Ltd. (n.d.). Human BAK1 ELISA kit instruction manual. FineTest.
2. Harris BHL, Macaulay VM, Harris DA. (2022). Obesity: A perfect storm for carcinogenesis. Cancer Metastasis Reviews. 41: 491-515. https://doi.org/10.1007/s10555-022-10046-2; PMid:36038791 PMCid:PMC9470699
3. Hooks O, Jhumkhawala V, Sibson K, Shrontz A, Krishnan SS, Ahmad S. (2025). Diabetes, obesity, and endometrial cancer: A review. Current Oncology. 32(12): 672. https://doi.org/10.3390/curroncol32120672; PMid:41440200 PMCid:PMC12732130
4. Huang P, Fan X, Yu H, Zhang K, Li H, Wang Y, Xue F. (2023). Glucose metabolic reprogramming and its therapeutic potential in obesity-associated endometrial cancer. Journal of Translational Medicine. 21(1): 94. https://doi.org/10.1186/s12967-022-03851-4; PMid:36750868 PMCid:PMC9906873
5. Liang L, Song C, Yang B, Chang C, Chen S, Sun L. (2025). Mapping the relationship between obesity and endometrial cancer: Current research hotspots and future trends (2003-2024). Frontiers in Oncology. 15: 1567022. https://doi.org/10.3389/fonc.2025.1567022; PMid:41114340 PMCid:PMC12527895
6. Ordeanu I-M, Busuioc CJ, Văduva C-C, Pană R-C, Petrescu A-M, Văruț RM et al. (2025). Obesity as a catalyst for endometrial hyperplasia and cancer progression: A narrative review of epidemiology, molecular pathways, and prevention. Biomedicines. 13: 2612. https://doi.org/10.3390/biomedicines13112612; PMid:41301707 PMCid:PMC12649901
7. Qian S, Wei Z, Yang W, Huang J, Yang Y, Wang J. (2022). The role of BCL-2 family proteins in regulating apoptosis and cancer therapy. Frontiers in Oncology. 12: 985363. https://doi.org/10.3389/fonc.2022.985363; PMid:36313628 PMCid:PMC9597512
8. Ray I, Meira LB, Michael A et al. (2022). Adipocytokines and disease progression in endometrial cancer: A systematic review. Cancer Metastasis Reviews. 41: 211-242. https://doi.org/10.1007/s10555-021-10002-6; PMid:34951691
9. Teede H, Khomami M, Morman R et al. (2026). Polyendocrine metabolic ovarian syndrome, the new name for polycystic ovary syndrome: A multistep global consensus process. The Lancet. (Advance online publication). https://doi.org/10.1016/S0140-6736(26)00717-8
10. Vaskivuo TE, Stenbäck F, Tapanainen JS. (2002). Apoptosis and apoptosis-related factors Bcl-2, Bax, tumor necrosis factor-α, and NF-κB in human endometrial hyperplasia and carcinoma. Cancer. 95(6): 1463-1471. https://doi.org/10.1002/cncr.10876; PMid:12237915
11. World Health Organization. (2024). Obesity and overweight. Retrieved from World Health Organization website.
