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Mints, Miriam
Publications (10 of 14) Show all publications
Govorov, I., Komlichenko, E., Ulrikh, E., Dikareva, E., Pervunina, T., Vazhenina, O., . . . Sitkin, S. (2025). The microbiome in endometrial cancer: vaginal milieu matters. Frontiers in Medicine, 12, Article ID 1533344.
Open this publication in new window or tab >>The microbiome in endometrial cancer: vaginal milieu matters
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2025 (English)In: Frontiers in Medicine, E-ISSN 2296-858X, Vol. 12, article id 1533344Article in journal (Refereed) Published
Abstract [en]

Endometrial cancer remains one of the most common malignancies in women, and its incidence is particularly increasing in developed countries. Despite the well-known promotive role of excessive exposure to estrogen, many other details of the pathogenesis of endometrial cancer remain unknown. Recent studies have elucidated the emerging role of the resident microbiota in the progression of various diseases, including cancer. Next-generation sequencing demonstrated that the uterine cavity, previously considered sterile, contains a composition-rich microbiota. In this work, we determined the differences in the composition of the intrauterine microbiota between patients with endometrial cancer and its precursor-endometrial hyperplasia.

Place, publisher, year, edition, pages
Frontiers Media S.A., 2025
Keywords
endometrial cancer, microbiota, endometrial microbiota, endometrial hyperplasia, carcinogenesis, vaginal microbiota
National Category
Cancer and Oncology
Identifiers
urn:nbn:se:oru:diva-121263 (URN)10.3389/fmed.2025.1533344 (DOI)001492680100001 ()40417664 (PubMedID)
Note

This work was financially supported by the Ministry of Science and Higher Education of the Russian Federation (Agreement No.075-15-2022-301). 

Available from: 2025-05-28 Created: 2025-05-28 Last updated: 2025-06-11Bibliographically approved
Castro Wersäll, O., Razumova, Z., Govorov, I. & Mints, M. (2023). Dietary Habits and Daily Routines as Prognostic Factors in Endometrial Cancer: A Machine Learning Approach. Nutrition and Cancer, 75(1), 310-319
Open this publication in new window or tab >>Dietary Habits and Daily Routines as Prognostic Factors in Endometrial Cancer: A Machine Learning Approach
2023 (English)In: Nutrition and Cancer, ISSN 0163-5581, E-ISSN 1532-7914, Vol. 75, no 1, p. 310-319Article in journal (Refereed) Published
Abstract [en]

Endometrial cancer (EC) is becoming more common worldwide, primarily due to an increase in life expectancy and obesity. As several modifiable factors may affect EC incidence and progression, we aimed to elucidate how dietary habits and daily routines influence recurrence and survival among women with EC, using a Random Survival Forest (RSF) approach. 481 women who previously underwent hysterectomy due to EC completed two extensive questionnaires on dietary habits and daily routines, and we used RSF to identify risky or protective variables. Among the 186 variables considered, consumption of sugar-sweetened beverages and fried potatoes increased the risk of EC recurrence and death, while physical activity decreased the risk of death. We conclude that RSF is a suitable approach to study survival in multivariable datasets.

Place, publisher, year, edition, pages
Routledge, 2023
National Category
Cancer and Oncology
Identifiers
urn:nbn:se:oru:diva-101426 (URN)10.1080/01635581.2022.2112241 (DOI)000854116000001 ()36104928 (PubMedID)2-s2.0-85138236083 (Scopus ID)
Funder
Stockholm County Council, FoUI-953093Swedish Research Council, OLL 935942
Available from: 2022-09-23 Created: 2022-09-23 Last updated: 2023-12-08Bibliographically approved
Dominguez-Valentin, M., Mints, M. & Moller, P. (2023). Mortality by age, gene and gender in carriers of pathogenic mismatch repair gene variants receiving surveillance for early cancer diagnosis and treatment: a report from the prospective Lynch syndrome database. eClinicalMedicine, 58, Article ID 101909.
Open this publication in new window or tab >>Mortality by age, gene and gender in carriers of pathogenic mismatch repair gene variants receiving surveillance for early cancer diagnosis and treatment: a report from the prospective Lynch syndrome database
2023 (English)In: eClinicalMedicine, E-ISSN 2589-5370, Vol. 58, article id 101909Article in journal (Refereed) Published
Abstract [en]

BACKGROUND: The Prospective Lynch Syndrome Database (PLSD) collates information on carriers of pathogenic or likely pathogenic MMR variants (path_MMR) who are receiving medical follow-up, including colonoscopy surveillance, which aims to the achieve early diagnosis and treatment of cancers. Here we use the most recent PLSD cohort that is larger and has wider geographical representation than previous versions, allowing us to present mortality as an outcome, and median ages at cancer diagnoses for the first time.

METHODS: The PLSD is a prospective observational study without a control group that was designed in 2012 and updated up to October 2022. Data for 8500 carriers of path_MMR variants from 25 countries were included, providing 71,713 years of follow up. Cumulative cancer incidences at 65 years of age were combined with 10-year crude survival following cancer, to derive estimates of mortality up to 75 years of age by organ, gene, and gender.

FINDINGS: Gynaecological cancers were more frequent than colorectal cancers in path_MSH2, path_MSH6 and path_PMS2 carriers [cumulative incidence: 53.3%, 49.6% and 23.3% at 75 years, respectively]. Endometrial, colon and ovarian cancer had low mortality [8%, 13% and 15%, respectively] and prostate cancers were frequent in male path_MSH2 carriers [cumulative incidence: 39.7% at 75 years]. Pancreatic, brain, biliary tract and ureter and kidney and urinary bladder cancers were associated with high mortality [83%, 66%, 58%, 27%, and 29%, respectively]. Among path_MMR carriers undergoing colonoscopy surveillance, particularly path_MSH2 carriers, more deaths followed non-colorectal Lynch syndrome cancers than colorectal cancers.

INTERPRETATION: In path_MMR carriers undergoing colonoscopy surveillance, non-colorectal Lynch syndrome cancers were associated with more deaths than were colorectal cancers. Reducing deaths from non-colorectal cancers presents a key challenge in contemporary medical care in Lynch syndrome.

FUNDING: We acknowledge funding from the Norwegian Cancer Society, contract 194751-2017.

Place, publisher, year, edition, pages
Elsevier, 2023
Keywords
Cancer risk, Lynch syndrome, MLH1, MSH2, MSH6, Mortality, PMS2, Prospective study, Survival
National Category
Cancer and Oncology
Identifiers
urn:nbn:se:oru:diva-113096 (URN)10.1016/j.eclinm.2023.101909 (DOI)001021447500001 ()37181409 (PubMedID)2-s2.0-85153285119 (Scopus ID)
Note

Funding Agency:

Norwegian Cancer Society

Available from: 2024-04-12 Created: 2024-04-12 Last updated: 2024-04-12Bibliographically approved
Razumova, Z., Govorov, I., Östensson, E. & Mints, M. (2022). Cadmium Intake as a Prognostic Factor in Endometrial Cancer: A Swedish Cohort-Based Study. Nutrition and Cancer, 74(1), 175-184
Open this publication in new window or tab >>Cadmium Intake as a Prognostic Factor in Endometrial Cancer: A Swedish Cohort-Based Study
2022 (English)In: Nutrition and Cancer, ISSN 0163-5581, E-ISSN 1532-7914, Vol. 74, no 1, p. 175-184Article in journal (Refereed) Published
Abstract [en]

Metalloendocrinology is a new interdisciplinary field, which was established due to the importance of connections between inorganic chemicals and hormonal mechanisms. The role of cadmium in hormone-related tumors is an excellent example of this connection, as cadmium mimics estrogen in the human body. Since endometrial cancer (EC) is hormone-related, it is well-suited for assessing the estrogenic effects of cadmium. Therefore, the present study aims to explore the role of dietary cadmium intake in the progression-free survival (PFS) and overall survival (OS) in women with EC. Dietary cadmium intake was estimated based on a large cohort of Swedish women (n = 416) with EC. Median dietary cadmium intake was then analyzed in relation to different tumor characteristics and clinical outcomes. Cox proportional hazard models were used to estimate hazard ratios (HRs) and 95% confidence intervals (CIs). Median daily dietary cadmium intake in the cohort was 13.1 μg (interquartile range 25%-75%=6.4). High dietary cadmium intake (μg/day) was associated with significantly decreased OS in the study cohort (HR = 0.956, 95% CI = 0.914-1.001, p = 0.05). Dietary cadmium intake was not associated with PFS (HR = 0.975, 95% CI = 0.924-1.028, p = 0.348). Therefore, our results indicate that high dietary cadmium intake could be associated with poor outcome in women with EC.

Place, publisher, year, edition, pages
Routledge, 2022
National Category
Nutrition and Dietetics Cancer and Oncology
Identifiers
urn:nbn:se:oru:diva-89745 (URN)10.1080/01635581.2021.1883681 (DOI)000619047900001 ()33593165 (PubMedID)2-s2.0-85116680712 (Scopus ID)
Available from: 2021-02-18 Created: 2021-02-18 Last updated: 2025-02-11Bibliographically approved
Belkić, K., Andersson, S., Alder, S., Mints, M. & Megyessi, D. (2022). Predictors of treatment failure for adenocarcinoma in situ of the uterine cervix: Up to 14 years of recorded follow-up. Oncology Letters, 24(4), Article ID 357.
Open this publication in new window or tab >>Predictors of treatment failure for adenocarcinoma in situ of the uterine cervix: Up to 14 years of recorded follow-up
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2022 (English)In: Oncology Letters, ISSN 1792-1074, E-ISSN 1792-1082, Vol. 24, no 4, article id 357Article in journal (Refereed) Published
Abstract [en]

The incidence of adenocarcinoma-in-situ (AIS) of the uterine cervix is rising, with invasive adenocarcinoma becoming increasingly common relative to squamous cell carcinoma. The present study reviewed a cohort of 84 patients first-time treated by conization for histologically-confirmed AIS from January 2001 to January 2017, to identify risk factors associated with recurrent/persistent AIS as well as progression to invasive cervical cancer. Nearly 80% of the patients were age 40 or younger at conization. Endocervical and ectocervical margins were deemed clear in 42 of the patients. All but two patients had ≥1 follow-up, with post-conization high-risk human papilloma virus (HPV) results documented in 52 patients. Altogether, 12 histopathologically-confirmed recurrences (14.3%) were detected; two of these patients had microinvasive or invasive carcinoma. In three other patients cytology showed AIS, but without recorded histopathology. Eight patients underwent hysterectomy for incomplete resection very soon after primary conization; they were not included in bivariate or multivariate analyses. Having ≥1 post-follow-up positive HPV finding yielded the highest sensitivity for histologically-confirmed recurrence: 87.5 [95% confidence interval (CI) 47.4-99.7]. Current or historical smoking status provided highest specificity: 94.4 (95% CI 72.7-99.9) and overall accuracy: 88.0 (95% CI 68.8-97.5) for histologically-confirmed recurrence. With multiple logistic regression (MLR), adjusting for age at conization and abnormal follow-up cytology, positive HPV18 was the strongest predictor of histologically-confirmed recurrence (P<0.005). Having ≥2 positive HPV results also predicted recurrence (P<0.02). Any unclear margin yielded an odds ratio 7.21 (95% CI 1.34-38.7) for histologically-confirmed recurrence adjusting for age, but became non-significant when including abnormal cytology in the MLR model. The strong predictive value of HPV, particularly HPV18 and persistent HPV positivity vis-à-vis detected recurrence indicated that regular HPV testing for patients treated for AIS is imperative. In conclusion, furthering a participatory approach, including attention to smoking with encouragement to attend needed long-term follow-up, can better protect these patients at high risk for cervical cancer.

Place, publisher, year, edition, pages
Spandidos Publications, 2022
Keywords
Adenocarcinoma-in-situ, margin status, papillomavirus infection, treatment failure
National Category
Cancer and Oncology
Identifiers
urn:nbn:se:oru:diva-101539 (URN)10.3892/ol.2022.13477 (DOI)000861095000001 ()36168314 (PubMedID)2-s2.0-85138642321 (Scopus ID)
Available from: 2022-09-29 Created: 2022-09-29 Last updated: 2023-07-03Bibliographically approved
Govorov, I., Attarha, S., Kovalevska, L., Andersson, E., Kashuba, E. & Mints, M. (2022). STK4 protein expression pattern follows different trends in endometrioid and serous endometrial adenocarcinoma upon tumor progression. Scientific Reports, 12(1), Article ID 22154.
Open this publication in new window or tab >>STK4 protein expression pattern follows different trends in endometrioid and serous endometrial adenocarcinoma upon tumor progression
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2022 (English)In: Scientific Reports, E-ISSN 2045-2322, Vol. 12, no 1, article id 22154Article in journal (Refereed) Published
Abstract [en]

In a previous study, we showed that serine/threonine-protein kinase 4 (STK4) is involved in the control on proliferation and migration of endometrial cancer (EC) cells in vitro. In the present paper, we studied STK4 expression in EC tissues from a large cohort of patients to determine whether STK4 can serve as a marker for the aggressiveness and prognosis of EC. Tissue samples from patients with EC were examined for tumor type, grade, and stage. The STK4 protein expression in EC cells was assessed by immunohistochemistry and related to clinicopathological data of patients, such as progression and patient survival rate. The STK4 mRNA levels and its relation to the survival rate were analyzed also in publicly available databases. The STK4 gene expression was low at both, the mRNA and protein levels in EC, especially in serous tumors. Comparison of STK4 expression with the patient survival rate shows that the higher expression is associated with worse prognosis in serous EC, while no such dependence was found in endometrioid EC. Hence, the determination of the SKT4 expression pattern could be used as a putative prognostic marker for serous EC.

Place, publisher, year, edition, pages
Nature Publishing Group, 2022
National Category
Cancer and Oncology
Identifiers
urn:nbn:se:oru:diva-103142 (URN)10.1038/s41598-022-26391-9 (DOI)000905026500002 ()36550267 (PubMedID)2-s2.0-85144578328 (Scopus ID)
Funder
Karolinska Institute, 562083Stockholm County CouncilThe Cancer Research Funds of Radiumhemmet, 151202
Note

Funding agency:

National Academy of Science of Ukraine 2.2.5.384 

Available from: 2023-01-16 Created: 2023-01-16 Last updated: 2024-04-08Bibliographically approved
Govorov, I., Attarha, S., Kovalevska, L., Andersson, E., Kashuba, E. & Mints, M. (2022). Upregulation of PKN1 as a Prognosis Biomarker for Endometrial Cancer. Cancer Control: Journal of the Moffitt Cancer Cente, 29, Article ID 10732748221094797.
Open this publication in new window or tab >>Upregulation of PKN1 as a Prognosis Biomarker for Endometrial Cancer
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2022 (English)In: Cancer Control: Journal of the Moffitt Cancer Cente, ISSN 1073-2748, E-ISSN 1526-2359, Vol. 29, article id 10732748221094797Article in journal (Refereed) Published
Abstract [en]

BACKGROUND: Several markers of survival among endometrial cancer (EC) patients have been proposed, namely, the oncoprotein stathmin, RAF kinase inhibitor (RKIP), Cyclin A, GATA-binding protein 3 (GATA3), and growth and differentiation factor-15 (GDF-15). Their elevated expression correlated significantly with a high stage, serous papillary/clear cell subtypes, and aneuploidy. In a previous study, we reported the elevated expression of the serine/threonine protein kinase N1 (PKN1) in cancerous cells. In the present paper, we studied PKN1 expression in EC tissues from a large cohort of patients, to determine whether PKN1 can serve as a marker for the aggressiveness and prognosis of EC, and/or as a marker of survival among EC patients.

METHODS: Tissue samples from EC patients were examined retrospectively for tumor type, tumor size, FIGO stage and grade, depth of invasion in the myometrium, and presence of lymph node metastasis. The PKN1 protein expression in EC cells was assessed by immunohistochemistry. PKN1 mRNA levels were analyzed in publicly available databases, using bioinformatic tools.

RESULTS: We found that expression of PKN1 at the mRNA and proteins levels tended to increase in high-grade EC samples (P = .0001 and P = .06, respectively). In addition, patients with metastatic disease had higher PKN1 mRNA levels (P = .02). Moreover, patients with high PKN1 expression could be characterized by poorer survival.

CONCLUSIONS: We have shown a trend of the higher PKN1 expression levels in EC patients with poor prognosis. Therefore, PKN1 might be considered as a candidate prognostic marker for EC.

Place, publisher, year, edition, pages
Sage Publications, 2022
Keywords
PKN1, endometrial cancer, prognostic marker, survival, tumor progression
National Category
Cancer and Oncology
Identifiers
urn:nbn:se:oru:diva-98917 (URN)10.1177/10732748221094797 (DOI)000797516900001 ()35533253 (PubMedID)2-s2.0-85129489856 (Scopus ID)
Funder
Stockholm County Council, 562083Karolinska Institute, 562083
Note

Funding agencies:

Cancer Research Foundation (Radiumhemmets Forskningsfonder) 151202

Research Program 2.2.5.384 of NAS of Ukraine

Available from: 2022-05-10 Created: 2022-05-10 Last updated: 2022-05-31Bibliographically approved
Andersson, S., Belkić, K., Mints, M. & Östensson, E. (2021). Acceptance of Self-Sampling Among Long-Term Cervical Screening Non-Attenders with HPV-Positive Results: Promising Opportunity for Specific Cancer Education. Journal of Cancer Education, 36(1), 126-133
Open this publication in new window or tab >>Acceptance of Self-Sampling Among Long-Term Cervical Screening Non-Attenders with HPV-Positive Results: Promising Opportunity for Specific Cancer Education
2021 (English)In: Journal of Cancer Education, ISSN 0885-8195, E-ISSN 1543-0154, Vol. 36, no 1, p. 126-133Article in journal (Refereed) Published
Abstract [en]

This study aims to investigate acceptance of vaginal self-sampling for high-risk human papilloma virus (HPV) among long-term screening non-attenders at increased cervical cancer risk and to identify leverage points to promote screening adherence among these women. Forty-three long-term screening non-attenders performed home vaginal self-sampling for HPV, had positive HPV results, and subsequently attended gynecologic examination. Sixteen (37.2%) had high-grade cervical intraepithelial neoplasia (CIN2 or 3), and two had invasive cervical cancer. Forty-one of these women completed a questionnaire concerning Specific Knowledge about HPV, CIN, and cervical cancer, potential barriers to screening and views about self-sampling. Results were compared with 479 women treated for CIN2+ who attended gynecologic follow-up and also performed self-sampling. Significant multivariate predictors of long-term non-attender status compared with referents were low Specific Knowledge, high confidence in self-sampling, and potential barriers-refraining from activity to attend gynecologic examination, needing another's help to attend, and long travel time. Non-attenders citing fear/refraining from gynecologic examination as why they preferred self-sampling significantly more often had lowest Specific Knowledge compared with other non-attenders. All non-attenders could envision themselves doing self-sampling again while only 74% of referents endorsed this statement (p = 0.0003). We conclude that HPV self-sampling is an acceptable option for women at increased cervical cancer risk who have been long-term screening non-attenders. Educational outreach to enhance Specific Knowledge about HPV, CIN and cervical cancer is critical. Those non-attenders who explicitly avoid gynecologic examinations need special attention. Trial Registry: Clinicaltrials.gov NCT02750124.

Place, publisher, year, edition, pages
Springer, 2021
Keywords
Cervical cancer screening, HPV testing, Leverage points, Selfcollection, Specific knowledge
National Category
Cancer and Oncology
Identifiers
urn:nbn:se:oru:diva-78277 (URN)10.1007/s13187-019-01608-0 (DOI)000575368800001 ()31522376 (PubMedID)2-s2.0-85073941330 (Scopus ID)
Funder
The Karolinska Institutet's Research FoundationSwedish Cancer Society, 11 0544 CAN 2011/471Swedish Research Council, 5212008-2899
Note

Funding Agencies:

Medical Research Council UK (MRC) LS 2015-1198

Cancer Society in Stockholm  154022

Available from: 2019-11-28 Created: 2019-11-28 Last updated: 2023-12-08Bibliographically approved
Andersson, S., Megyessi, D., Belkic, K., Alder, S., Östensson, E. & Mints, M. (2021). Age, margin status, high-risk human papillomavirus and cytology independently predict recurrent high-grade cervical intraepithelial neoplasia up to 6 years after treatment. Oncology Letters, 22(3), Article ID 684.
Open this publication in new window or tab >>Age, margin status, high-risk human papillomavirus and cytology independently predict recurrent high-grade cervical intraepithelial neoplasia up to 6 years after treatment
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2021 (English)In: Oncology Letters, ISSN 1792-1074, E-ISSN 1792-1082, Vol. 22, no 3, article id 684Article in journal (Refereed) Published
Abstract [en]

The present study aimed to identify the factors that independently contribute to disease recurrence among women first-time treated for high-grade cervical intraepithelial neoplasia (CIN) during 4-6 years of follow-up. Overall, 529 of 530 eligible patients participated; these patients all attended a 1st follow-up appointment similar to 6 months post-conization, at which time high-risk human-papillomavirus (HPV) testing, liquid-based cytology and colposcopy were performed. Full data on margin excision status, other aspects of initial treatment and comorbidity were obtained. At least one subsequent follow-up was attended by 88% of patients. A total of 22 recurrent cases were detected during follow-up. Detected recurrence was the outcome of focus for multiple logistic regression analysis, with odds ratios (OR) and 95% confidence intervals (CI) computed. Four significant independent risk factors were identified: Age 45 years or above (OR=3.5, 95% CI=1.3-9.9), one or both unclear or uncertain margins (OR=5.3, 95% CI=2.0-14.2), positive HPV at 1st follow-up (OR=5.8, 95% CI=2.0-16.8), and abnormal cytology at 1st follow-up (OR=3.9, 95% CI=1.4-11.0). Bivariate analysis revealed that persistent HPV positivity was associated with recurrence (P<0.01). These findings indicated that incomplete excision of the CIN lesion may warrant more intensive subsequent screening, regardless of early post-conization HPV findings. Although early post-conization positive HPV was a powerful, independent predictor of recurrent high-grade CIN, over one-third of the patients with detected recurrence had a negative early post-conization HPV finding. These patients returned for routine screening, at which time, in most cases, HPV status was positive, thus indicating the need for repeated HPV evaluation. Especially during the on-going pandemic, home vaginal self-sampling is recommended. Particular attention is required for women aged >= 45 years. In addition, although not statistically significant, relevant comorbidities, especially autoimmune conditions, warrant consideration in clinical decision-making. Women who have been treated for high-grade CIN are at risk for recurrent disease and progression to cervical cancer; therefore, they require careful, individualized follow-up to avoid these adverse consequences.

Place, publisher, year, edition, pages
Spandidos Publications, 2021
Keywords
cervical intraepithelial neoplasia, treatment failure, margin status, papillomavirus infection, age
National Category
Cancer and Oncology
Identifiers
urn:nbn:se:oru:diva-93745 (URN)10.3892/ol.2021.12945 (DOI)000681340600001 ()34434283 (PubMedID)2-s2.0-85111553773 (Scopus ID)
Funder
Swedish Cancer Society, 110544 CAN2011/471The Karolinska Institutet's Research Foundation, 5888/05-722Swedish Research Council, 521-2008-2899European CommissionStockholm County Council, 20130097
Available from: 2021-08-19 Created: 2021-08-19 Last updated: 2021-08-27Bibliographically approved
Wersäll, O. C., Löfstedt, L., Govorov, I., Mints, M., Gabrielson, M. & Shoshan, M. (2021). PGC1α and VDAC1 expression in endometrial cancer. Molecular and clinical oncology, 14(2), Article ID 42.
Open this publication in new window or tab >>PGC1α and VDAC1 expression in endometrial cancer
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2021 (English)In: Molecular and clinical oncology, ISSN 2049-9450, E-ISSN 2049-9469, Vol. 14, no 2, article id 42Article in journal (Refereed) Published
Abstract [en]

Endometrial cancer (EC) is one of the ten most common gynecological cancers. As in most cancers, EC tumour progression involves alterations in cellular metabolism and can be associated with, for instance, altered levels of glycolytic enzymes. Mitochondrial functions and proteins are known to serve key roles in tumour metabolism and progression. The transcriptional coactivator peroxisome proliferator-activated receptor gamma coactivator 1 (PGC1α) is a major regulator of mitochondrial biogenesis and function, albeit of varying prognostic value in different cancers. The voltage-dependent anion channel type 1 (VDAC1) regulates apoptosis as well as metabolite import and export over the mitochondrial outer membrane, and is often used for comparative quantification of mitochondrial content. Using immunohistochemistry, the present study examined protein expression levels of PGC1α and VDAC1 in tumour and paired benign tissue samples from 148 patients with EC, in order to examine associations with clinical data, such as stage and grade, Ki-67, p53 status, clinical resistance and overall survival. The expression levels of both PGC1α and VDAC1, as well as a PGC1α downstream effector, were significantly lower in tumor tissues than in benign tissues, suggesting altered mitochondrial function in EC. However, Kaplan-Meier, log rank and Spearman's rank correlation tests revealed that their expression was not correlated with survival and clinical data. Therefore, PGC1α and VDAC1 are not of major prognostic value in EC.

Place, publisher, year, edition, pages
Spandidos Publications, 2021
Keywords
endometrial cancer, mitochondria, peroxisome proliferator-activated receptor gamma coactivator 1, voltage-dependent anion channel type 1, prognosis
National Category
Cancer and Oncology
Identifiers
urn:nbn:se:oru:diva-88496 (URN)10.3892/mco.2020.2203 (DOI)000607955300001 ()33437480 (PubMedID)2-s2.0-85099121751 (Scopus ID)
Funder
Swedish Cancer Society, 140373Stockholm County Council, SLL-562083
Available from: 2021-01-15 Created: 2021-01-15 Last updated: 2021-01-29Bibliographically approved
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