دورية أكاديمية
The Subtype Identity of Testicular Cancer Cells Determines Their Immunostimulatory Activity in a Coculture Model.
العنوان: | The Subtype Identity of Testicular Cancer Cells Determines Their Immunostimulatory Activity in a Coculture Model. |
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المؤلفون: | Gayer FA; Institute for Cellular and Molecular Immunology, University Medical Center Göttingen, 37073 Göttingen, Germany.; Clinic of Urology, University Medical Center Göttingen, 37075 Göttingen, Germany., Henkel M; Institute for Cellular and Molecular Immunology, University Medical Center Göttingen, 37073 Göttingen, Germany., Luft J; Institute for Cellular and Molecular Immunology, University Medical Center Göttingen, 37073 Göttingen, Germany., Reichardt SD; Institute for Cellular and Molecular Immunology, University Medical Center Göttingen, 37073 Göttingen, Germany., Fichtner A; Institute of Pathology, University Medical Center Göttingen, 37075 Göttingen, Germany., Legler TJ; Department of Transfusion Medicine, University Medical Center Göttingen, 37075 Göttingen, Germany., Reichardt HM; Institute for Cellular and Molecular Immunology, University Medical Center Göttingen, 37073 Göttingen, Germany. |
المصدر: | Cancers [Cancers (Basel)] 2023 May 05; Vol. 15 (9). Date of Electronic Publication: 2023 May 05. |
نوع المنشور: | Journal Article |
اللغة: | English |
بيانات الدورية: | Publisher: MDPI Country of Publication: Switzerland NLM ID: 101526829 Publication Model: Electronic Cited Medium: Print ISSN: 2072-6694 (Print) Linking ISSN: 20726694 NLM ISO Abbreviation: Cancers (Basel) Subsets: PubMed not MEDLINE |
أسماء مطبوعة: | Original Publication: Basel, Switzerland : MDPI |
مستخلص: | Testicular germ cell cancer (TGCC) is subdivided into several subtypes. While seminomatous germ cell tumors (SGCT) are characterized by an intensive infiltration of immune cells which constitute a pro-inflammatory tumor micromilieu (TME), immune cells in non-seminomatous germ cell tumors (NSGCT) are differently composed and less abundant. Previously, we have shown that the seminomatous cell line TCam-2 promotes T cell and monocyte activation in a coculture model, resulting in mutual interactions between both cell types. Here we set out to compare this feature of TCam-2 cells with the non-seminomatous cell line NTERA-2. Peripheral blood T cells or monocytes cocultured with NTERA-2 cells failed to secrete relevant amounts of pro-inflammatory cytokines, and significantly downregulated the expression of genes encoding activation markers and effector molecules. In contrast, immune cells cocultured with TCam-2 cells produced IL-2, IL-6 and TNFα, and strongly upregulated the expression of multiple pro-inflammatory genes. Furthermore, the expression of genes involved in proliferation, stemness and subtype specification remained unaltered in NTERA-2 cells during coculture with T cells or monocytes, indicating the absence of mutual interactions. Collectively, our findings uncover fundamental differences between SGCT and NSGCT in their capability to generate a pro-inflammatory TME, which possibly impacts the clinical features and prognosis of both TGCC subtypes. |
References: | Int J Cancer. 2020 Mar 15;146(6):1592-1605. (PMID: 31583686) Cell Tissue Res. 2008 Feb;331(2):529-38. (PMID: 18008088) Int J Androl. 2007 Aug;30(4):350-65. (PMID: 17705808) Oncoimmunology. 2017 Mar 20;6(4):e1305535. (PMID: 28507813) Cancers (Basel). 2022 Aug 19;14(16):. (PMID: 36011006) Curr Med Chem. 2018;25(36):4785-4806. (PMID: 28707587) Genes Chromosomes Cancer. 2008 Mar;47(3):185-96. (PMID: 18050305) Crit Rev Oncol Hematol. 2007 Dec;64(3):182-97. (PMID: 17644403) Br J Cancer. 2022 Apr;126(6):937-947. (PMID: 35022523) Eur Urol. 2015 Dec;68(6):1054-68. (PMID: 26297604) Am J Surg Pathol. 2006 Jul;30(7):858-65. (PMID: 16819328) Pigment Cell Melanoma Res. 2015 Sep;28(5):490-500. (PMID: 25818762) Semin Immunol. 2014 Feb;26(1):38-47. (PMID: 24602448) Immunol Invest. 1995 May;24(4):607-18. (PMID: 7622197) Nat Rev Cancer. 2005 Mar;5(3):210-22. (PMID: 15738984) Int J Mol Sci. 2021 Jun 29;22(13):. (PMID: 34209703) Cells. 2022 Mar 04;11(5):. (PMID: 35269507) Oncogene. 2003 Mar 27;22(12):1880-91. (PMID: 12660824) Andrology. 2017 Jul;5(4):763-770. (PMID: 28544640) Hum Reprod. 2016 Oct;31(10):2192-202. (PMID: 27609978) J Reprod Immunol. 2013 Dec;100(2):135-45. (PMID: 24290033) Oncology (Williston Park). 2002 Feb;16(2):217-26, 229; discussion 230-2. (PMID: 11866137) J Immunother Cancer. 2017 Mar 21;5:28. (PMID: 28331617) Mech Dev. 2005 Sep;122(9):1034-42. (PMID: 16023837) J Proteome Res. 2019 Apr 5;18(4):1819-1826. (PMID: 30835130) Urology. 2013 Feb;81(2):464.e1-9. (PMID: 23374840) Rev Sci Tech. 1998 Apr;17(1):84-94. (PMID: 9638802) Eur J Immunol. 2017 Jul;47(7):1232-1242. (PMID: 28555838) Oncotarget. 2016 Jul 26;7(30):47095-47110. (PMID: 27283990) Histopathology. 2021 Mar;78(4):593-606. (PMID: 32970854) J Hematol Oncol. 2021 Mar 19;14(1):45. (PMID: 33741032) Hum Cell. 2020 Oct;33(4):930-937. (PMID: 32507979) Dis Markers. 2019 Sep 3;2019:8298524. (PMID: 31565104) Cancer Biol Ther. 2010 Sep 15;10(6):529-36. (PMID: 20855948) BMC Clin Pathol. 2012 Oct 15;12:19. (PMID: 23066729) Eur J Cancer. 2020 Jun;132:127-135. (PMID: 32361383) PLoS One. 2014 Jan 03;9(1):e83585. (PMID: 24404135) Genes Chromosomes Cancer. 2012 Jul;51(7):717-26. (PMID: 22489004) Int J Cancer. 1999 Dec 10;83(6):815-22. (PMID: 10597201) |
معلومات مُعتمدة: | Scholarship Deutsche Forschungsgemeinschaft; RE 1631/17-1 Deutsche Forschungsgemeinschaft |
فهرسة مساهمة: | Keywords: NTERA-2; T cell; TCam-2; cytokines; inflammation; monocyte; non-seminoma; seminoma; testicular germ cell cancer; tumor microenvironment |
تواريخ الأحداث: | Date Created: 20230513 Latest Revision: 20230515 |
رمز التحديث: | 20231215 |
مُعرف محوري في PubMed: | PMC10177190 |
DOI: | 10.3390/cancers15092619 |
PMID: | 37174085 |
قاعدة البيانات: | MEDLINE |
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