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Evaluation of BRIP-1 (FANCJ) and FANCI Protein Expression in Ovarian Cancer Tissue.

作者信息

Kozłowski Mateusz, Borzyszkowska Dominika, Golara Anna, Durys Damian, Piotrowska Katarzyna, Kempińska-Podhorodecka Agnieszka, Cymbaluk-Płoska Aneta

机构信息

Department of Reconstructive Surgery and Gynecological Oncology, Pomeranian Medical University in Szczecin, Al. Powstańców Wielkopolskich 72, 70-111 Szczecin, Poland.

Department of Physiology, Pomeranian Medical University, 70-111 Szczecin, Poland.

出版信息

Biomedicines. 2024 Nov 21;12(12):2652. doi: 10.3390/biomedicines12122652.


DOI:10.3390/biomedicines12122652
PMID:39767562
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11673538/
Abstract

Ovarian cancer is one of the most common cancers in women. Markers associated with ovarian cancer are still being sought. The aim of this study was to evaluate the expression of BRIP-1 (FANCJ) and FANCI proteins in ovarian cancer tissue and to assess these expressions in differentiating the described clinical features. The study enrolled 68 patients with ovarian cancer. The cohort was divided into a HGSOC (high-grade serous ovarian cancer) group and a non-HGSOC group, which represented ovarian cancer other than HGSOC. Immunohistochemical evaluation of FANCI and BRIP-1 (FANCJ) protein expression in ovarian cancer tissue samples was performed. All statistical analyses were performed using StatView software (Carry, NC, USA). The FANCI protein mostly showed moderate positive and strong positive expression, while BRIP-1 protein mostly showed no expression or positive expression. Patients with lower expression of FANCI and BRIP-1 showed differences in the clinical stage of HGSOC, which was not observed in patients with higher expression of these proteins. In addition, patients with lower BRIP-1 expression showed differences in menopausal status, which was not observed in patients with higher expression of this protein. This study shows that FANCI protein is a marker associated with lower FIGO stage and histologically high-grade cancer in a group of all ovarian cancers and in non-HGSOC.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ab9/11673538/473629c7344f/biomedicines-12-02652-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ab9/11673538/d9167263d1e8/biomedicines-12-02652-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ab9/11673538/2bccb325ffd0/biomedicines-12-02652-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ab9/11673538/28bb2414076b/biomedicines-12-02652-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ab9/11673538/447ba24c4334/biomedicines-12-02652-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ab9/11673538/065162a2a99c/biomedicines-12-02652-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ab9/11673538/df5c45120b8d/biomedicines-12-02652-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ab9/11673538/473629c7344f/biomedicines-12-02652-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ab9/11673538/d9167263d1e8/biomedicines-12-02652-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ab9/11673538/2bccb325ffd0/biomedicines-12-02652-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ab9/11673538/28bb2414076b/biomedicines-12-02652-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ab9/11673538/447ba24c4334/biomedicines-12-02652-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ab9/11673538/065162a2a99c/biomedicines-12-02652-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ab9/11673538/df5c45120b8d/biomedicines-12-02652-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ab9/11673538/473629c7344f/biomedicines-12-02652-g007.jpg

相似文献

[1]
Evaluation of BRIP-1 (FANCJ) and FANCI Protein Expression in Ovarian Cancer Tissue.

Biomedicines. 2024-11-21

[2]
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J Cancer Res Clin Oncol. 2019-2-27

[3]
Differences between complex epithelial neoplasms of the ovary and high-grade serous ovarian cancer: a retrospective observational cohort study.

J Ovarian Res. 2022-12-1

[4]
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Rom J Morphol Embryol. 2020

[5]
Circular RNA profiling reveals circRNA1656 as a novel biomarker in high grade serous ovarian cancer.

Biosci Trends. 2019-4-24

[6]
Prognostic value of kallikrein-related peptidase 7 (KLK7) mRNA expression in advanced high-grade serous ovarian cancer.

J Ovarian Res. 2020-10-21

[7]
The Prognostic Significance of Tumor-Infiltrating Lymphocytes, PD-L1, BRCA Mutation Status and Tumor Mutational Burden in Early-Stage High-Grade Serous Ovarian Carcinoma-A Study by the Spanish Group for Ovarian Cancer Research (GEICO).

Int J Mol Sci. 2023-7-6

[8]
[Study of the clinical significance of ETAR mRNA expression in high-grade serous ovarian cancer and the inhibitory effect of ETAR derived fusion polypeptide on cancer progression].

Zhonghua Fu Chan Ke Za Zhi. 2023-12-25

[9]
Increased expression of IDO1 is associated with improved survival and increased number of TILs in patients with high-grade serous ovarian cancer.

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[10]
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本文引用的文献

[1]
FANCI Inhibition Induces PARP1 Redistribution to Enhance the Efficacy of PARP Inhibitors in Breast Cancer.

Cancer Res. 2024-10-15

[2]
Senaparib as first-line maintenance therapy in advanced ovarian cancer: a randomized phase 3 trial.

Nat Med. 2024-6

[3]
FANCI serve as a prognostic biomarker correlated with immune infiltrates in skin cutaneous melanoma.

Front Immunol. 2023

[4]
Early-Onset Ovarian Cancer <30 Years: What Do We Know about Its Genetic Predisposition?

Int J Mol Sci. 2023-11-30

[5]
Fanconi anemia pathway regulation by FANCI in prostate cancer.

Front Oncol. 2023-10-30

[6]
High-grade serous ovarian carcinoma, the "Achiles' hill" for clinicians and molecular biologists: a molecular insight.

Mol Biol Rep. 2023-11

[7]
FANCI is Associated with Poor Prognosis and Immune Infiltration in Liver Hepatocellular Carcinoma.

Int J Med Sci. 2023

[8]
Molecular Genetic Characteristics of , a Proposed New Ovarian Cancer Predisposing Gene.

Genes (Basel). 2023-1-20

[9]
Germline and somatic variants in ovarian carcinoma: A next-generation sequencing (NGS) analysis.

Front Oncol. 2022-12-1

[10]
State of the science: Contemporary front-line treatment of advanced ovarian cancer.

Gynecol Oncol. 2022-7

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