Expression of the immune checkpoint receptor TIGIT in seminoma
Open accessAbstract
A characteristic feature of testicular seminoma is the abundance of immune cells in the tumor microenvironment, raising the possibility that immune checkpoint inhibitors may serve as a therapeutic option in these types of tumors. T cell immunoreceptor with Ig and ITIM domains (TIGIT) is an inhibitory immune checkpoint receptor in analogy to PD‑1, and drugs targeting TIGIT are currently being investigated in clinical trials. Little is known about the expression of these proteins in testicular seminomas. Therefore the present study performed immunohistochemical analysis to determine the relative abundance of TIGIT and PD‑1 in relation to the total CD3+ immune cell infiltration in a tissue microarray (TMA) constructed from 78 seminoma patients. The fraction of TIGIT+ and PD‑1+ lymphocytes was highly variable in individual cancers and ranged from 2.3 to 69.4% (mean: 32.2±14.7%) for TIGIT and from 0.8 to 56.5% (mean: 21.6±13.2%) for PD‑1. The same high degree of variability was also identified for the ratio of PD‑1 to TIGIT positive cells, which varied from a dominance of TIGIT (PD‑1: TIGIT ratio=0.02) in 74% of patients, to a predominance of PD‑1 (PD‑1: TIGIT ratio=12.5) in 23% of patients. In summary, the immune checkpoint receptors TIGIT and PD‑1 are abundantly expressed in human seminomas. Once available, anti‑TIGIT antibodies, possibly in combination with anti‑PD‑1 drugs, may be a reasonable therapeutic strategy for this type of cancer.
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In seminoma samples, several immune checkpoint receptors are overexpressed in the cancerous cells.
“A recent immunohistochemical analysis of seminoma samples revealed the overexpression of several immune checkpoint receptors in the cancerous cells.”
From The Immune Landscape and Immunotherapeutic Strategies in Platinum-Refractory Testicular Germ Cell Tumors (2024) · cites this paper as [57]
The Results (page unavailable) report TIGIT and PD-1 staining in immune cells within all 78 seminomas, not overexpression in the cancerous cells. The Introduction likewise says the study examined these receptors on lymphocytes. The claim assigns the finding to the wrong cell type. (LLM, conf=0.88)
Checked by a reasoning model — may be wrong.
Experimental — accuracy not yet measuredTIGIT is significantly overexpressed in seminoma samples.
“Notably, TIGIT (T-cell immunoreceptor with Ig and ITIM domains) was found to be significantly overexpressed [57].”
From The Immune Landscape and Immunotherapeutic Strategies in Platinum-Refractory Testicular Germ Cell Tumors (2024) · cites this paper as [57]
The Results report TIGIT-positive lymphocytes in all 78 seminomas, and the Discussion describes TIGIT expression in their tumor-infiltrating T cells. The paper reports variable abundance, but does not establish statistically significant overexpression against a specified comparator. (LLM, conf=0.88)
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Cites
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Cited by
Sorted by citations
Evmorfopoulos, K., Marsitopoulos, K., Karachalios, R., Karathanasis, A., Dimitropoulos, K., Tzortzis, V., Zachos, I., & Vlachostergios, P. J. (2024) · Cancers · doi:10.3390/cancers16020428 · Cited by 11 · see citing works
“Notably, TIGIT (T-cell immunoreceptor with Ig and ITIM domains) was found to be significantly overexpressed [57].”
Background
- Authors
- Hinsch, A., Blessin, N., Simon, R., Kluth, M., Fischer, K., Hube‑Magg, C., Li, W., Makrypidi‑Fraune, G., Wellge, B., Mandelkow, T., Debatin, N., H�flmayer, D., Lennartz, M., Sauter, G., Izbicki, J., Minner, S., B�scheck, F., Uhlig, R., Dum, D., Krech, T., Luebke, A., Wittmer, C., Jacobsen, F., Burandt, E., Steurer, S., & Wilczak, W.
- Affiliations
- University Medical Center Hamburg-Eppendorf (DE)
- Hochschule für bildende Künste (DE)
- Department of Pathology, University Medical Center Hamburg‑Eppendorf, D‑20246 Hamburg, Germany
- Corresponding author
- Simon, Ronald
- ORCID
- Venue
- Oncology Letters
- Publisher
- Spandidos Publications
- Published
- 2019-05-31
- Volume
- 18
- Issue
- 2
- Pages
- 1497-1502
- ISSN
- 1792-1074 (ISSN-L)
- 1792-1082
- PMC
- PMC6607271
- OpenAlex
- W2947677762
- Cited by
- 12
- References
- 5
- Citations by year
- 2025: 2 · 2024: 2 · 2023: 2 · 2021: 2 · 2020: 3 · 2019: 1
- FWCI
- 0.63
- Type
- journal article
- Language
- en
- Open access
- diamond
- doi.org
- Licence
- cc-by-nc-nd
- Locations
- Oncology Letters (publishedVersion, cc-by-nc-nd)
- Europe PMC (PubMed Central) (publishedVersion, cc-by-nc-nd)
- PubMed Central (publishedVersion, cc-by-nc-nd)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Oncology › Cancer Immunotherapy and Biomarkers
- Health Sciences › Medicine › Surgery › Testicular diseases and treatments
- Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
- Keywords
- TIGIT, PD-1, seminoma, immune checkpoint receptors, tumor microenvironment, CD3+ T cell infiltration, immune checkpoint inhibitors, anti-PD-1 combination therapy
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