Dergiler / Türkderm-Deri Hastalıkları ve Frengi Arşivi / 2018 / Cilt: 52 - Sayı: 4

Is there any association between mycosis fungoides and Th-1, Th-2 cytokines and transforming growth factor-beta 1 gene polymorphisms?

Mikozis fungoides ile Th-1, Th-2 sitokinleri ve transforming growth factor-beta 1 gen polimorfizmleri arasında herhangi bir ilişki var mıdır?

Sayfa
137–141
DOI
—
🏛️Bu makalenin bibliyografik verileri ve tam metin bağlantısı DergiPark üzerinden sağlanmıştır.
DergiPark Kaydı ↗
✨

Yapay Zeka Hızlı Bakış & Çıkarımlar

AI Insight
⚡ TL;DR(1 Cümlede Hızlı Çıkarım)

There was no significant difference between advanced stage and early stage cases and healthy controls.Conclusion: None of the studied cytokine gene polymorphisms are risk factors for the development or progression of MF in the Turkishpopulation, however, further studies are needed.

📌 3 Maddede Bu Makale

🎯
Amaç & Hipotez:Background and Design: Cytokines are considered to play a crucial role in the development of mycosis fungoides (MF).
📊
Temel Bulgular & Veri:The aim of thisstudy was to determine any possible cytokine gene polymorphisms that may be a risk factor for the development or progression of MF.Materials and Methods: Genotyping of interferon-gamma (IFN-γ)+874, interleukin (IL)-10-1082, IL-6-174, transforming growth factor-beta 1(TGF-β1), codon 10 and codon 25, and tumor necrosis factor-alpha (TNF-α)-308 was undertaken in 55 Turkish patients with MF and comparedto 50 healthy controls.
💡
Sonuç & Katkı:There was no significant difference between advanced stage and early stage cases and healthy controls.Conclusion: None of the studied cytokine gene polymorphisms are risk factors for the development or progression of MF in the Turkishpopulation, however, further studies are needed.
🔬Tür:Araştırma Makalesi
📍Kapsam:Genişletilmiş Akademik Örneklem
⚙️Değişkenler:Alan Parametreleri

Özet

Background and Design: Cytokines are considered to play a crucial role in the development of mycosis fungoides (MF). Cytokine productionis under genetic control and allelic variations of cytokine genes are associated with lower or higher production of cytokines. The aim of thisstudy was to determine any possible cytokine gene polymorphisms that may be a risk factor for the development or progression of MF.Materials and Methods: Genotyping of interferon-gamma (IFN-γ)+874, interleukin (IL)-10-1082, IL-6-174, transforming growth factor-beta 1(TGF-β1), codon 10 and codon 25, and tumor necrosis factor-alpha (TNF-α)-308 was undertaken in 55 Turkish patients with MF and comparedto 50 healthy controls. Polymerase chain reaction (PCR)-restriction fragment length polymorphism was applied for IFN-γ+874, IL-10-1082, IL-6-174 and TNF-α-308 gene polymorphisms. TGF-β1 was genotyped by direct DNA sequencing of PCR amplified gene products for codon 10and codon 25 polymorphisms.Results: Genotype distributions showed no significant difference between the patients and the controls for any of the five investigatedcytokines. There was no significant difference between advanced stage and early stage cases and healthy controls.Conclusion: None of the studied cytokine gene polymorphisms are risk factors for the development or progression of MF in the Turkishpopulation, however, further studies are needed.

Abstract

Amaç: Sitokinlerin mikozis fungoides (MF) gelişiminde önemli rol oynadığı düşünülmektedir. Sitokin üretimi genetik kontrol altındadır ve sitokin genlerinin allelik varyasyonları düşük veya yüksek sitokin üretimi ile ilişkilidir. Bu çalışmanın amacı MF gelişimi veya progresyonunda risk faktörü olabilecek herhangi bir sitokin gen polimorfizminin belirlenmesidir. Gereç ve Yöntem: Interferon-gamma (IFN-γ)+874, interlökin (IL)-10-1082, IL-6-174, transforme edici büyüme faktör-beta 1 (TGF-β1) kodon 10 ve kodon 25 ve tümör nekroz faktörü-alfa (TNF-α)-308’in genotiplemesi, MF'li 55 Türk hastada yapıldı ve 50 sağlıklı kontrol ile karşılaştırıldı. IFN-γ+ 874, IL-10-1082, IL-6-174 ve TNF-α-308 gen polimorfizmleri için polimeraz zincirleme reaksiyonu (PCR) - kısıtlama parçası uzunluk polimorfizmi uygulandı. TGF-β1, kodon 10 ve kodon 25 polimorfizmleri PCR ile çoğaltılmış gen ürünlerinin doğrudan DNA dizilemesi ile genotiplendi. Bulgular: Araştırılan beş sitokinden herhangi birinin genotip dağılımı hasta ve kontrol grubu arasında anlamlı farklılık göstermedi. İleri evre ve erken evre olgular ve sağlıklı kontroller arasında anlamlı fark yoktu. Sonuç: Çalışılan sitokin gen polimorfizmlerinin hiçbiri, Türk popülasyonunda MF gelişimi veya progresyonu için risk faktörleri değildir, bununla birlikte daha ileri çalışmalara ihtiyaç vardır.

🔖

Bu Makaleye Atıf Yap

YAZİCİ, S., AYDOĞAN, K., SARICAOĞLU, H., BAŞKAN, E. B., TUNALI, Ş. (2018). Is there any association between mycosis fungoides and Th-1, Th-2 cytokines and transforming growth factor-beta 1 gene polymorphisms?. Türkderm-Deri Hastalıkları ve Frengi Arşivi, Cilt: 52 - Sayı: 4, 137–141. https://ajindex.com/articles/417145

📄 Tam Metin PDF Okuyucu

📄

PDF görüntüleyici hazırlanıyor...

Kaynakça (13)

  1. Nadeem A, Mumtaz S, Naveed AK, et al: Gene-gene, gene-environment, gene-nutrient interactions and single nucleotide polymorphisms of inflammatory cytokines. World J Diabetes 2015;6:642-7.
  2. Hollegaard MV, Bidwell JL: Cytokine gene polymorphism in human disease: on-line databases, Supplement 3. Genes Immun 2006;7:269-76.
  3. McGirt LY, Jia P, Baerenwald DA, et al: Whole-genome sequencing reveals oncogenic mutations in mycosis fungoides. Blood 2015;126:508-19.
  4. Jawed SI, Myskowski PL, Horwitz S, Moskowitz A, Querfeld C: Primary cutaneous T-cell lymphoma (mycosis fungoides and Sézary syndrome): part I. Diagnosis: clinical and histopathologic features and new molecular and biologic markers. J Am Acad Dermatol 2014;70:205. Tan RS, Butterworth CM, McLaughlin H, Malka S, Samman PD. Mycosis fungoides--a disease of antigen persistence. Br J Dermatol 1974;91:607-11.
  5. Beyer M, Möbs M, Humme D, Sterry W: Pathogenesis of mycosis fungoides. J Dtsch Dermatol Ges 2011;9:594-8.
  6. Wu PA, Huang V, Bigby ME: Interventions for mycosis fungoides: critical commentary on a Cochrane Systematic Review. Br J Dermatol 2014;170:1015-20.
  7. Olsen E, Vonderheid E, Pimpinelli N, et al: ISCL/EORTC. Revisions to the staging and classification of mycosis fungoides and Sezary syndrome: a proposal of the International Society for Cutaneous Lymphomas (ISCL) and the cutaneous lymphoma task force of the European Organization of Research and Treatment of Cancer (EORTC). Blood 2007;110:1713-22.
  8. Morse HR, Olomolaiye OO, Wood NA, Keen LJ, Bidwell JL: Induced heteroduplex genotyping of TNF-alpha, IL-1beta, IL-6 and IL-10 polymorphisms associated with transcriptional regulation. Cytokine 1999;11:789-95.
  9. Ohtsuka T, Yamakage A, Yamazaki S: The polymorphism of transforming growth factor-beta1 gene in Japanese patients with systemic sclerosis. Br J Dermatol 2002;147:458-63
  10. Smith AJ, Humphries SE: Cytokine and cytokine receptor gene polymorphisms and their functionality. Cytokine Growth Factor Rev 2009;20:43-59.
  11. Lan Q, Wang SS, Menashe I, et al: Genetic variation in Th1/Th2 pathway genes and risk of non-Hodgkin lymphoma: a pooled analysis of three population- based case-control studies. Br J Haematol 2011;153:341-50.
  12. Gu X, Shen Y, Fu L, et al: Polymorphic variation of inflammation-related genes and risk of non-Hodgkin lymphoma for Uygur and Han Chinese in Xinjiang. Asian Pac J Cancer Prev 2014;15:9177-83.
  13. Colakogullari M, Ulukaya E, Yilmaztepe Oral A, et al: The involvement of IL-10, IL-6, IFN-gamma, TNF-alpha and TGF-