Journals / Bağcılar Tıp Bülteni / 2021 / Cilt: 6 - Sayı: 2

Immunohistochemical Analysis of1.25-dihydroxyvitamin D3 Receptor Expression inEndometrial Cancer

Endometrium Kanserinde 1,25-dihidroksivitamin D3 Reseptör Ekspresyonunun İmmünohistokimyasal Analizi

Pages
142–147
Publication Date
2022-10-12
DOI
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

The intensity of expression, extent of staining and overall scores were determined for the semi-quantitative evaluation of VDR expression.

📌 3 Key Takeaways

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Objective & Hypothesis:Objective: This study aimed to immunohistochemically investigate the expression of 1.25-dihydroxyvitamin-D3-receptors (VDR) in benign and malignant lesions of the endometrial tissue.Method: The cases were divided into two groups as benign (n=10) and endometrioid adenocarcinoma (n=17) according to their endometrial pathology results.
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Key Findings & Data:The expression of VDR was examined by immunohistochemical method in endometrial tissues of participants (n=27).
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Conclusion & Impact:The intensity of expression, extent of staining and overall scores were determined for the semi-quantitative evaluation of VDR expression.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Objective: This study aimed to immunohistochemically investigate the expression of 1.25-dihydroxyvitamin-D3-receptors (VDR) in benign and malignant lesions of the endometrial tissue.Method: The cases were divided into two groups as benign (n=10) and endometrioid adenocarcinoma (n=17) according to their endometrial pathology results. The expression of VDR was examined by immunohistochemical method in endometrial tissues of participants (n=27). Then, VDR expression levels were compared between the groups. The intensity of expression, extent of staining and overall scores were determined for the semi-quantitative evaluation of VDR expression. Demographic data of the patients were also recorded.Results: There was no significant difference between the groups in terms of demographic data (p>0.05) except age (p

Özet

Amaç: Bu çalışma, endometrial dokunun benign ve malign lezyonlarında1,25-dihidroksi-vitamin-D3-reseptörlerinin (VDR) ekspresyonunuimmünohistokimyasal olarak araştırmak için tasarlandı. Yöntem: Olgular endometrial patoloji sonuçlarına göre benign (n=10)ve endometrioid adenokarsinom (n=17) olarak iki gruba ayrıldı.Olgulara (n=27) ait olan endometrial dokulardaki VDR ekspresyonuimmünohistokimyasal yöntemlerle incelendi ve gruplar arasında VDRekspresyon seviyeleri karşılaştırıldı. VDR ekspresyonunun yarı niceldeğerlendirilmesi için ekspresyon yoğunluğu, boyanma dansitesi vegenel skorlar belirlendi. Hastalara ait demografik veriler kaydedildi. Bulgular: Gruplar arasında, yaş dışındaki (p0,05). Malign grupta VDR ekspresyon düzeyi benigngruba göre anlamlı olarak daha yüksekti (p

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Cite This Article

ÇETİN, N. K., TURAN, Ö. D. (2022). Immunohistochemical Analysis of1.25-dihydroxyvitamin D3 Receptor Expression inEndometrial Cancer. Bağcılar Tıp Bülteni, Cilt: 6 - Sayı: 2, 142–147. https://ajindex.com/articles/458913

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References (14)

  1. Stewart BW, Wild C. World cancer report: Cancer Worldwide. 3rd ed. Lyon, France: Non-Series Publications; 2014:12-18
  2. Purdie DM, Green AC. Epidemiology of endometrial cancer. Best Pract Res Clin Obstet Gynaecol 2001;15(3):341-354
  3. Miettinen S, Ahonen MH, Lou YR, Manninen T, Tuohimaa P, Syvala H, et al. Role of 24-hydroxylase in vitamin D3 growth response of OVCAR-3 ovarian cancer cells. Int J Cancer 2004;108(3):367-373
  4. Ziegler RG, Jones CJ, Brinton LA, Norman SA, Mallin K, Levine RS, et al. Diet and the risk of in situ cervical cancer among white women in the United States. Cancer Causes Control 1991;2(1):17- 29
  5. Garland CF, Garland FC, Gorham ED, Lipkin M, Newmark H, Mohr SB, et al. The role of vitamin D in cancer prevention. Am J Public Health 2006;96(2):252-261
  6. Pittas AG, Chung M, Trikalinos T, Joanna Mitri J, Brendel M, Patel K, et al. Systematic review: Vitamin D and cardiometabolic outcomes. Ann Intern Med 2010;152(5):307-314
  7. Kim JS, Kim YI, Song C, Yoon I, Park JW, Choi YB, et al. Association of vitamin D receptor gene polymorphism and Parkinson’s disease in koreans. J Korean Med Sci 2005;20(3):495-498
  8. Zhang J, Chalmers MJ, Stayrook KR, Burris LL, Wang Y, Busby SA, et al. DNA binding alters coactivator interaction surfaces of the intact vdr-rxr complex. Nat Struct Mol Biol 2011;18(5):556-563
  9. Ferlay J, Soerjomataram I, Dikshit R, Eser S, Mathers C, Rebelo M, et al. Cancer incidence and mortality worldwide: Sources, methods and major patterns in globocan 2012. Int J Cancer 2015;136(5):E359-E386
  10. Deuster E, Jeschke U, Ye Y, Mahner S, Czogalla B. Vitamin D and VDR in gynecological cancers - a systematic review. Int J Mol Sci 2017;18(11):2328
  11. Agic A, Xu H, Altgassen C, Noack F, Monika M, Wolfler MM, et al. Relative expression of 1,25-dihydroxyvitamin d3 receptor,vitamin d 1α-hydroxylase, vitamin d 24- hydroxylase, and vitamin d 25-hydroxylase in endometriosis and gynecologic cancers. Reprod Sci 2007;14(5):486-497
  12. Bergada L, Pallares J, Arcidiacono MV, Cardus A, Santacana M, Valls J, et al. Role of local bioactivation of vitamin D by CYP27A1 and CYP2R1 in the control of cell growth in normal endometrium and endometrial carcinoma. Lab Invest 2014;94(6):608-622
  13. Zhigang Z, Wenlv S. Prostate stem cell antigen (PSCA) expression in human prostate cancer tissues: implications for prostate carcinogenesis and progression of prostate cancer. Jpn J Clin Oncol 2004;34(7):414-419
  14. Mohr SB, Garland CF, Gorham ED, G