Abstract 309: Oncogenic cooperation of MUC13 and NDRG1 signaling in liver cancer.

Abstract Background: Liver cancer is one of the leading causes of cancer-related mortality worldwide, highlighting the vital importance of understanding its molecular mechanism for the development of targeted therapies. Mucin 13 (MUC13), a transmembrane glycoprotein, has been associated with the oncogenic processes that cause liver cancer. Our previous studies have shown its significance in promoting cancer cell survival, proliferation, and metastasis. Emerging evidence indicates that NDRG1 (N-Myc downstream regulated gene 1), played a critical role in cell growth, development, stress response, invasion and migration, may also be implicated in the pathogenesis of liver cancer. The current study aims to investigate the influence of the co-expression of MUC13 and NDRG1 on liver cancer progression and determine if their co-expression is correlated with clinical outcomes. Methodology: We employed liver cancer cell lines corresponding to different tumor grades characterized by MUC13 positivity. The expression levels of MUC13 and NDRG1 were evaluated in these cell lines. We performed confocal microscopy for immunofluorescence to examine co-localization of MUC13 and NDRG1. Furthermore, we conducted immunohistochemical analysis of MUC13-positive patient samples to evaluate NDRG1 expression levels. We additionally examined public databases to assess the correlation of NDRG1 and MUC13 expressions with patient survival. Results: We identified a notable association between increased levels of MUC13 expression and elevated NDRG1 expression in MUC13-positive liver cancer cell lines, suggesting a potential interplay that may facilitate cancer progression. Immunofluorescence assays performed on these cell lines provided yields strong evidence of co-localization between MUC13 and NDRG1. Additionally, our studies demonstrated a direct molecular interaction between MUC13 and NDRG1 in liver cancer cells as evidenced by proximity ligation assay (PLA). We further confirmed NDRG1 expression in MUC13-positive and negative patient samples through immunohistochemical staining. To corroborate our findings, we conducted a correlational analysis using public clinical database, which revealed an association between NDRG1 and MUC13 expression levels, suggesting that higher co-expression of these two molecules is linked to poor overall survival (OS) rates. Conclusion: The outcomes of this study indicate a notable co-expression of MUC13 and NDRG1 in liver cancer, potentially highlighting their cooperative involvement in tumor progression. Citation Format: Shabnam Malik, Mohammed Sikander, Daniel Zubieta, Mirza Sarwar Baig, Iris Enriquez, Murali M. Yallapu, Subhash C. Chauhan. Oncogenic cooperation of MUC13 and NDRG1 signaling in liver cancer [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 309.

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Journal
Cancer Research
Published
2026-04-03
DOI
https://doi.org/10.1158/1538-7445.am2026-309
Primary Topic
Mechanisms of cancer metastasis
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article
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article

Abstract 309: Oncogenic cooperation of MUC13 and NDRG1 signaling in liver cancer.

Mirza Sarwar Baig, Mohammed Sikander, Murali Mohan Yallapu, Daniel Zubieta et al.
Cancer Research
Mechanisms of cancer metastasis
article

Abstract 309: Oncogenic cooperation of MUC13 and NDRG1 signaling in liver cancer.

Mirza Sarwar Baig, Mohammed Sikander, Murali Mohan Yallapu, Daniel Zubieta, Shabnam Malik, Iris Enriquez, Subhash C. Chauhan
article en

Abstract

Abstract Background: Liver cancer is one of the leading causes of cancer-related mortality worldwide, highlighting the vital importance of understanding its molecular mechanism for the development of targeted therapies. Mucin 13 (MUC13), a transmembrane glycoprotein, has been associated with the oncogenic processes that cause liver cancer. Our previous studies have shown its significance in promoting cancer cell survival, proliferation, and metastasis. Emerging evidence indicates that NDRG1 (N-Myc downstream regulated gene 1), played a critical role in cell growth, development, stress response, invasion and migration, may also be implicated in the pathogenesis of liver cancer. The current study aims to investigate the influence of the co-expression of MUC13 and NDRG1 on liver cancer progression and determine if their co-expression is correlated with clinical outcomes. Methodology: We employed liver cancer cell lines corresponding to different tumor grades characterized by MUC13 positivity. The expression levels of MUC13 and NDRG1 were evaluated in these cell lines. We performed confocal microscopy for immunofluorescence to examine co-localization of MUC13 and NDRG1. Furthermore, we conducted immunohistochemical analysis of MUC13-positive patient samples to evaluate NDRG1 expression levels. We additionally examined public databases to assess the correlation of NDRG1 and MUC13 expressions with patient survival. Results: We identified a notable association between increased levels of MUC13 expression and elevated NDRG1 expression in MUC13-positive liver cancer cell lines, suggesting a potential interplay that may facilitate cancer progression. Immunofluorescence assays performed on these cell lines provided yields strong evidence of co-localization between MUC13 and NDRG1. Additionally, our studies demonstrated a direct molecular interaction between MUC13 and NDRG1 in liver cancer cells as evidenced by proximity ligation assay (PLA). We further confirmed NDRG1 expression in MUC13-positive and negative patient samples through immunohistochemical staining. To corroborate our findings, we conducted a correlational analysis using public clinical database, which revealed an association between NDRG1 and MUC13 expression levels, suggesting that higher co-expression of these two molecules is linked to poor overall survival (OS) rates. Conclusion: The outcomes of this study indicate a notable co-expression of MUC13 and NDRG1 in liver cancer, potentially highlighting their cooperative involvement in tumor progression. Citation Format: Shabnam Malik, Mohammed Sikander, Daniel Zubieta, Mirza Sarwar Baig, Iris Enriquez, Murali M. Yallapu, Subhash C. Chauhan. Oncogenic cooperation of MUC13 and NDRG1 signaling in liver cancer [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 309.

Cancer ResearchVol. 86(7_Supplement)
Jamia Hamdard (IN), The University of Texas Rio Grande Valley (US)
Good health and well-being
Openalex Percentile: Top 7%
Mechanisms of cancer metastasis
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