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Non-Hodgkin Lenfoma’lı Hastaların Serum İnterlökin-36 Alfa, Beta, Gamma ve İnterlökin-17 Düzeylerinin Belirlenmesi

Year 2025, Issue: Early Access
https://doi.org/10.18678/dtfd.1555362

Abstract

Amaç: Non-Hodgkin lenfoma (NHL), lenfoid hücrelerin kontrolsüz çoğalmasıyla tanımlanan çeşitli bir hematolojik kanser grubudur. Bu çalışmanın amacı, NHL hastalarında immün sistemde önemli bir rol oynayan interlökin-36 alfa (IL-36α), interlökin-36 beta (IL-36β), interlökin-36 gama (IL-36γ) ve interlökin-17 (IL-17) serum konsantrasyonları arasındaki ilişkiyi ve bu sitokinlerin NHL için potansiyel biyobelirteçler veya tedavi hedefleri olarak hizmet edip edemeyeceğini değerlendirmektir.
Gereç ve Yöntemler: Çalışmaya Sivas Cumhuriyet Üniversitesi Tıp Fakültesi Hematoloji bölümünde tanı almış ve takip edilmiş 55 NHL hastası ve 33 sağlıklı kontrol olmak üzere toplam 88 birey dahil edildi. Hastaların tanı anındaki ve kontrol grubundaki bireylerin hemogram ve biyokimya tetkikleri ile serum IL-17, IL-36α, IL-36β ve IL-36γ düzeylerinin çalışılması için kan örnekleri alındı. Hastalar interim pozitron emisyon tomografisi/bilgisayarlı tomografi (PET/BT) sonuçlarına göre komplet remisyon (CR), parsiyel remisyon (PR) ve progresyon olmak üzere üç gruba ayrıldı.
Bulgular: Serum IL-36α (p<0,001), IL-36β (p=0,022), IL-36γ (p<0,001) ve IL-17 (p<0,001) konsantrasyonları NHL hastalarında sağlıklı kontrollere kıyasla istatistiksel olarak anlamlı derecede daha yüksekti. Progresyon gösteren hastalarda IL-17, IL-36α, IL-36β ve IL-36γ düzeyleri CR ve PR gruplarına göre daha düşük olmasına rağmen bu farklar istatistiksel olarak anlamlı değildi (sırasıyla p=0,065; p=0,186; p=0,151 ve p=0,065).
Sonuç: Bu sitokinler NHL’nin etyopatogenezi ve hatta progresyonu üzerinde etkili olabilir. Ancak, NHL oldukça heterojen bir hastalık grubunu oluşturduğundan, daha geniş kapsamlı in-vivo ve in-vitro çalışmalara ihtiyaç vardır.

References

  • Howlader N, Morton LM, Feuer EJ, Besson C, Engels EA. Contributions of subtypes of non-Hodgkin lymphoma to mortality trends. Cancer Epidemiol Biomarkers Prev. 2016;25(1):174-9.
  • Moubadder L, McCullough LE, Flowers CR, Koff JL. Linking environmental exposures to molecular pathogenesis in non-Hodgkin lymphoma subtypes. Cancer Epidemiol Biomarkers Prev. 2020;29(10):1844-55.
  • Yuan ZC, Xu WD, Liu XY, Liu XY, Huang AF, Su LC. Biology of IL-36 signaling and its role in systemic inflammatory diseases. Front Immunol. 2019;10:2532.
  • Wang X, Yi P, Liang Y. The role of IL-36 in infectious diseases: a potential target for COVID-19? Front Immunol. 2021;12:662266.
  • Yang B, Kang H, Fung A, Zhao H, Wang T, Ma D. The role of interleukin 17 in tumor proliferation, angiogenesis, and metastasis. Mediators Inflamm. 2014;2014:623759.
  • Sheu BC, Chang WC, Cheng CY, Lin HH, Chang DY, Huang SC. Cytokine regulation networks in the cancer microenvironment. Front Biosci. 2008;13:6255-68.
  • Ding L, Wang X, Hong X, Lu L, Liu D. IL-36 cytokines in autoimmunity and inflammatory disease. Oncotarget. 2018;9(2):2895-901.
  • Shahzadi M, Ahmed D, Sawani S, Moosajee M. Outcome of primary CNS lymphoma; a retrospective analysis. Asian Pac J Cancer Care. 2022;7(1):41-6.
  • Shingleton J, Wang J, Baloh C, Dave T, Davis N, Happ L, et al. Non-Hodgkin lymphomas: Malignancies arising from mature B cells. Cold Spring Harb Perspect Med. 2021;11(3):a034843.
  • Terzi H, Oral K, Yılmaz H, Demir Yurtseven E, Şencan M. Single-center experience in relapsed/refractory non-Hodgkin’s lymphoma. Cumhuriyet Med J. 2022;44(1):51-6.
  • Neurath MF. IL-36 in chronic inflammation and cancer. Cytokine Growth Factor Rev. 2020;55:70-9.
  • Baker K, O’Donnell C, Bendix M, Keogh S, Byrne J, O’Riordain M, et al. IL-36 signalling enhances a pro-tumorigenic phenotype in colon cancer cells with cancer cell growth restricted by administration of the IL-36R antagonist. Oncogene. 2022;41(19):2672-84.
  • Zhang R, Jiang M, Huang M, Yang J, Liu Q, Zhao Z, et al. Prognostic value of Interleukin-36s in cancers: A systematic review and meta-analysis. Cytokine. 2023;172:156397.
  • Bilge Y, Terzi H, Doğan HO, Kablan D, Şencan M. Determination of serum interleukin-36 alpha, beta, gamma and interleukin-17 levels in patients with multiple myeloma. Cumhuriyet Med J. 2024;46(1):57-65.
  • Liu L, He H, Xu D, Feng Y, Zhou H, Shi L, et al. Association between interleukin 36γ and tumor progression in non-small cell lung cancer. Oncol Lett. 2020;19(3):2457-65.
  • Wu F, Xu J, Huang Q, Han J, Duan L, Fan J, et al. The role of interleukin‐17 in lung cancer. Mediators Inflamm. 2016;2016:8494079.
  • Welte T, Zhang XH. Interleukin‐17 could promote breast cancer progression at several stages of the disease. Mediators Inflamm. 2015;2015:804347.
  • Lim EJ, Peh SC. Bone marrow and peripheral blood changes in non-Hodgkin's lymphoma. Singapore Med J. 2000;41(6):279-85.
  • Bari A, Tadmor T, Sacchi S, Marcheselli L, Liardo EV, Pozzi S, et al. Monocytosis has adverse prognostic significance and impacts survival in patients with T-cell lymphomas. Leuk Res. 2013;37(6):619-23.

Determination of Serum Interleukin-36 Alpha, Beta, Gamma, and Interleukin-17 Levels in Patients with Non-Hodgkin Lymphoma

Year 2025, Issue: Early Access
https://doi.org/10.18678/dtfd.1555362

Abstract

Aim: Non-Hodgkin lymphoma (NHL) is a diverse group of hematologic cancers characterized by uncontrolled proliferation of lymphoid cells. This study aimed to evaluate the relationship between serum concentrations of interleukin-36 alpha (IL-36α), interleukin-36 beta (IL-36β), interleukin-36 gamma (IL-36γ), and interleukin-17 (IL-17), which play an important role in the immune system, in NHL patients and whether these cytokines can serve as potential biomarkers or therapeutic targets for NHL.
Material and Methods: A total of 88 individuals, including 55 NHL patients diagnosed and followed up in the Department of Hematology, Sivas Cumhuriyet University Medical Faculty, and 33 healthy controls, were included in the study. Blood samples were collected from patients at the time of diagnosis and from individuals in the control group for hemogram and biochemistry tests and serum IL-17, IL-36α, IL-36β, and IL-36γ levels. Patients were divided into three groups, complete remission (CR), partial remission (PR), and progression according to interim positron emission tomography/computed tomography (PET/CT) results.
Results: Serum IL-36α (p<0.001), IL-36β (p=0.022), IL-36γ (p<0.001), and IL-17 (p<0.001) concentrations were statistically significantly higher in NHL patients compared to healthy controls. Although IL-17, IL-36α, IL-36β, and IL-36γ levels were lower in patients with progression compared to the CR and PR groups, these differences were not statistically significant (p=0.065, p=0.186, p=0.151, and p=0.065, respectively).
Conclusion: These cytokines may influence the etiopathogenesis and even the progression of NHL. However, since NHL constitutes a highly heterogeneous disease group, more extensive in-vivo and in-vitro studies are needed.

References

  • Howlader N, Morton LM, Feuer EJ, Besson C, Engels EA. Contributions of subtypes of non-Hodgkin lymphoma to mortality trends. Cancer Epidemiol Biomarkers Prev. 2016;25(1):174-9.
  • Moubadder L, McCullough LE, Flowers CR, Koff JL. Linking environmental exposures to molecular pathogenesis in non-Hodgkin lymphoma subtypes. Cancer Epidemiol Biomarkers Prev. 2020;29(10):1844-55.
  • Yuan ZC, Xu WD, Liu XY, Liu XY, Huang AF, Su LC. Biology of IL-36 signaling and its role in systemic inflammatory diseases. Front Immunol. 2019;10:2532.
  • Wang X, Yi P, Liang Y. The role of IL-36 in infectious diseases: a potential target for COVID-19? Front Immunol. 2021;12:662266.
  • Yang B, Kang H, Fung A, Zhao H, Wang T, Ma D. The role of interleukin 17 in tumor proliferation, angiogenesis, and metastasis. Mediators Inflamm. 2014;2014:623759.
  • Sheu BC, Chang WC, Cheng CY, Lin HH, Chang DY, Huang SC. Cytokine regulation networks in the cancer microenvironment. Front Biosci. 2008;13:6255-68.
  • Ding L, Wang X, Hong X, Lu L, Liu D. IL-36 cytokines in autoimmunity and inflammatory disease. Oncotarget. 2018;9(2):2895-901.
  • Shahzadi M, Ahmed D, Sawani S, Moosajee M. Outcome of primary CNS lymphoma; a retrospective analysis. Asian Pac J Cancer Care. 2022;7(1):41-6.
  • Shingleton J, Wang J, Baloh C, Dave T, Davis N, Happ L, et al. Non-Hodgkin lymphomas: Malignancies arising from mature B cells. Cold Spring Harb Perspect Med. 2021;11(3):a034843.
  • Terzi H, Oral K, Yılmaz H, Demir Yurtseven E, Şencan M. Single-center experience in relapsed/refractory non-Hodgkin’s lymphoma. Cumhuriyet Med J. 2022;44(1):51-6.
  • Neurath MF. IL-36 in chronic inflammation and cancer. Cytokine Growth Factor Rev. 2020;55:70-9.
  • Baker K, O’Donnell C, Bendix M, Keogh S, Byrne J, O’Riordain M, et al. IL-36 signalling enhances a pro-tumorigenic phenotype in colon cancer cells with cancer cell growth restricted by administration of the IL-36R antagonist. Oncogene. 2022;41(19):2672-84.
  • Zhang R, Jiang M, Huang M, Yang J, Liu Q, Zhao Z, et al. Prognostic value of Interleukin-36s in cancers: A systematic review and meta-analysis. Cytokine. 2023;172:156397.
  • Bilge Y, Terzi H, Doğan HO, Kablan D, Şencan M. Determination of serum interleukin-36 alpha, beta, gamma and interleukin-17 levels in patients with multiple myeloma. Cumhuriyet Med J. 2024;46(1):57-65.
  • Liu L, He H, Xu D, Feng Y, Zhou H, Shi L, et al. Association between interleukin 36γ and tumor progression in non-small cell lung cancer. Oncol Lett. 2020;19(3):2457-65.
  • Wu F, Xu J, Huang Q, Han J, Duan L, Fan J, et al. The role of interleukin‐17 in lung cancer. Mediators Inflamm. 2016;2016:8494079.
  • Welte T, Zhang XH. Interleukin‐17 could promote breast cancer progression at several stages of the disease. Mediators Inflamm. 2015;2015:804347.
  • Lim EJ, Peh SC. Bone marrow and peripheral blood changes in non-Hodgkin's lymphoma. Singapore Med J. 2000;41(6):279-85.
  • Bari A, Tadmor T, Sacchi S, Marcheselli L, Liardo EV, Pozzi S, et al. Monocytosis has adverse prognostic significance and impacts survival in patients with T-cell lymphomas. Leuk Res. 2013;37(6):619-23.
There are 19 citations in total.

Details

Primary Language English
Subjects ​Internal Diseases, Clinical Chemistry
Journal Section Research Article
Authors

Hatice Terzi 0000-0003-3471-1305

Ecem Demir 0000-0001-9714-0672

Halef Okan Dogan 0000-0001-8738-0760

Mehmet Şencan 0000-0002-1459-3906

Early Pub Date February 24, 2025
Publication Date
Submission Date September 24, 2024
Acceptance Date January 28, 2025
Published in Issue Year 2025 Issue: Early Access

Cite

APA Terzi, H., Demir, E., Dogan, H. O., Şencan, M. (2025). Determination of Serum Interleukin-36 Alpha, Beta, Gamma, and Interleukin-17 Levels in Patients with Non-Hodgkin Lymphoma. Duzce Medical Journal(Early Access). https://doi.org/10.18678/dtfd.1555362
AMA Terzi H, Demir E, Dogan HO, Şencan M. Determination of Serum Interleukin-36 Alpha, Beta, Gamma, and Interleukin-17 Levels in Patients with Non-Hodgkin Lymphoma. Duzce Med J. February 2025;(Early Access). doi:10.18678/dtfd.1555362
Chicago Terzi, Hatice, Ecem Demir, Halef Okan Dogan, and Mehmet Şencan. “Determination of Serum Interleukin-36 Alpha, Beta, Gamma, and Interleukin-17 Levels in Patients With Non-Hodgkin Lymphoma”. Duzce Medical Journal, no. Early Access (February 2025). https://doi.org/10.18678/dtfd.1555362.
EndNote Terzi H, Demir E, Dogan HO, Şencan M (February 1, 2025) Determination of Serum Interleukin-36 Alpha, Beta, Gamma, and Interleukin-17 Levels in Patients with Non-Hodgkin Lymphoma. Duzce Medical Journal Early Access
IEEE H. Terzi, E. Demir, H. O. Dogan, and M. Şencan, “Determination of Serum Interleukin-36 Alpha, Beta, Gamma, and Interleukin-17 Levels in Patients with Non-Hodgkin Lymphoma”, Duzce Med J, no. Early Access, February 2025, doi: 10.18678/dtfd.1555362.
ISNAD Terzi, Hatice et al. “Determination of Serum Interleukin-36 Alpha, Beta, Gamma, and Interleukin-17 Levels in Patients With Non-Hodgkin Lymphoma”. Duzce Medical Journal Early Access (February 2025). https://doi.org/10.18678/dtfd.1555362.
JAMA Terzi H, Demir E, Dogan HO, Şencan M. Determination of Serum Interleukin-36 Alpha, Beta, Gamma, and Interleukin-17 Levels in Patients with Non-Hodgkin Lymphoma. Duzce Med J. 2025. doi:10.18678/dtfd.1555362.
MLA Terzi, Hatice et al. “Determination of Serum Interleukin-36 Alpha, Beta, Gamma, and Interleukin-17 Levels in Patients With Non-Hodgkin Lymphoma”. Duzce Medical Journal, no. Early Access, 2025, doi:10.18678/dtfd.1555362.
Vancouver Terzi H, Demir E, Dogan HO, Şencan M. Determination of Serum Interleukin-36 Alpha, Beta, Gamma, and Interleukin-17 Levels in Patients with Non-Hodgkin Lymphoma. Duzce Med J. 2025(Early Access).