Abstract 2693: Elucidating the role of specific cancer testis antigens in the progression and development of hepatocellular carcinoma.

Abstract Hepatocellular carcinoma (HCC) is a primary type of liver cancer and the third leading cause of cancer-related deaths. Non-resolving liver inflammation caused by a variety of etiological factors, such as viral hepatitis infections or alcohol abuse, initiates the transition from fibrosis to cirrhosis, and finally to cancer. Due to poor late-stage survival rates, novel biomarkers and therapeutic targets are desperately needed to improve HCC patient outcomes. Potential candidates include a group of Cancer Testes Antigens (CTAs), a large group of tumor-associated antigens expressed in multiple tumor types. The melanoma-associated antigen (MAGE) subfamily of CTAs is overexpressed in HCC tumors and may drive tumor progression and tumorigenesis. However, little is known about the expression patterns of these CTAs in the multiple precursor liver diseases that contribute to HCC development, such as chronic hepatitis or cirrhosis. Furthermore, the mechanisms regulating the expression of these members in liver tissue prior to and following metastatic development have not been fully elucidated. Initial Enzyme-Linked Immunosorbent Assay (ELISA) results have demonstrated an autoimmune response to these proteins as tumor-associated antigens in serum from patients with precursor liver conditions. Using computational approaches, we have evaluated the expression patterns of these CTAs in publicly available liver disease transcriptomic datasets. The analyzed samples were stratified by disease etiology to provide a comprehensive view of the spectrum of the transition from healthy to diseased liver. Wet-lab approaches, including Immunohistochemistry (IHC), were employed to validate these responses at the protein level. Our findings indicate that MAGE subfamily CTAs are potential biomarkers of HCC development, with the activation of individual members varying during the transition from diseased liver to cancer. By elucidating the molecular mechanisms and pathways by which HCC-specific CTAs function, we will be able to develop them as diagnostic markers and therapeutic targets. Citation Format: Frida Mariana Delgadillo, Barbara Yang, Sabrina Stogoski, Shrikanth S. Gadad, Enrique I. Ramos. Elucidating the role of specific cancer testis antigens in the progression and development of hepatocellular carcinoma [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 2693.

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Journal
Cancer Research
Published
2026-04-03
DOI
https://doi.org/10.1158/1538-7445.am2026-2693
Primary Topic
Immunotherapy and Immune Responses
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article
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article

Abstract 2693: Elucidating the role of specific cancer testis antigens in the progression and development of hepatocellular carcinoma.

Barbara Yang, Enrique Ramos, Shrikanth S. Gadad, Frida Mariana Delgadillo et al.
Cancer Research
Immunotherapy and Immune Responses
article

Abstract 2693: Elucidating the role of specific cancer testis antigens in the progression and development of hepatocellular carcinoma.

Barbara Yang, Enrique Ramos, Shrikanth S. Gadad, Frida Mariana Delgadillo, Sabrina Stogoski
article en

Abstract

Abstract Hepatocellular carcinoma (HCC) is a primary type of liver cancer and the third leading cause of cancer-related deaths. Non-resolving liver inflammation caused by a variety of etiological factors, such as viral hepatitis infections or alcohol abuse, initiates the transition from fibrosis to cirrhosis, and finally to cancer. Due to poor late-stage survival rates, novel biomarkers and therapeutic targets are desperately needed to improve HCC patient outcomes. Potential candidates include a group of Cancer Testes Antigens (CTAs), a large group of tumor-associated antigens expressed in multiple tumor types. The melanoma-associated antigen (MAGE) subfamily of CTAs is overexpressed in HCC tumors and may drive tumor progression and tumorigenesis. However, little is known about the expression patterns of these CTAs in the multiple precursor liver diseases that contribute to HCC development, such as chronic hepatitis or cirrhosis. Furthermore, the mechanisms regulating the expression of these members in liver tissue prior to and following metastatic development have not been fully elucidated. Initial Enzyme-Linked Immunosorbent Assay (ELISA) results have demonstrated an autoimmune response to these proteins as tumor-associated antigens in serum from patients with precursor liver conditions. Using computational approaches, we have evaluated the expression patterns of these CTAs in publicly available liver disease transcriptomic datasets. The analyzed samples were stratified by disease etiology to provide a comprehensive view of the spectrum of the transition from healthy to diseased liver. Wet-lab approaches, including Immunohistochemistry (IHC), were employed to validate these responses at the protein level. Our findings indicate that MAGE subfamily CTAs are potential biomarkers of HCC development, with the activation of individual members varying during the transition from diseased liver to cancer. By elucidating the molecular mechanisms and pathways by which HCC-specific CTAs function, we will be able to develop them as diagnostic markers and therapeutic targets. Citation Format: Frida Mariana Delgadillo, Barbara Yang, Sabrina Stogoski, Shrikanth S. Gadad, Enrique I. Ramos. Elucidating the role of specific cancer testis antigens in the progression and development of hepatocellular carcinoma [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 2693.

Cancer ResearchVol. 86(7_Supplement)
The University of Texas at El Paso (US), The University of Texas Rio Grande Valley (US)
Good health and well-being
Openalex Percentile: Top 6%
Immunotherapy and Immune Responses
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