Abstract 5232: Tumor-adipose microenvironment drives progression in advanced oral squamous cell carcinoma

Abstract Advanced oral squamous cell carcinoma (OSCC) is an aggressive cancer with a recurrence rate of 40-60%, and lymph node metastasis (LNM) occurs in 50% of cases, serving as a critical prognostic factor. Recent evidence suggests that fatty acid oxidation (FAO) enhances cancer cell survival, invasiveness, and therapeutic resistance. OSCC's histological proximity to dense adipose tissue provides a unique opportunity for cancer cells to acquire energy from the adipose environment, underscoring the importance of elucidating the tumor-adipose interactions in OSCC progression and metastasis. In this study, we investigated the impact of the tumor-adipose microenvironment on OSCC progression, focusing on interactions between adipocytes and cancer cells. Human adipose-derived stem cells (ADSCs) were differentiated into adipocytes and co-cultured with the OSCC cell line YD10B for three weeks to induce cancer-associated adipocytes (CAAs). Co-cultured adipocytes exhibited fibroblast-like phenotypic changes, reduced expression of adipogenic differentiation markers, and increased free fatty acid release. Inflammatory cytokines (e.g., IL-6) and tumor-promoting proteins (e.g., IGFBP-2) were upregulated. YD10B cells exposed to co-cultured adipocytes showed enhanced proliferation, invasion, and epithelial-mesenchymal transition (EMT) signaling. Adipocytes and cancer cells both showed increased expression of matrix metalloproteinases (MMP-2 and MMP-9), indicating mutual reinforcement of tumor aggressiveness. Collectively, these findings indicate that adipocytes, through their interaction with OSCC cells, undergo changes to acquire a CAA-like phenotype , which support tumor progression by providing fatty acids as an energy source and promoting aggressive phenotypes, including proliferation, invasion, and LNM. Targeting tumor-adipocyte interactions could offer novel therapeutic strategies to mitigate OSCC progression and improve outcomes. Citation Format: Gyeongmin Kang, Mi Rim Lee, Sumin Kang, Yu-Sun Lee, Hye Won Shon, Jiyoung Lee, Sung Weon Choi, Sun Il Choi, Yun-Hee Kim. Tumor-adipose microenvironment drives progression in advanced oral squamous cell carcinoma [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2025; Part 1 (Regular Abstracts); 2025 Apr 25-30; Chicago, IL. Philadelphia (PA): AACR; Cancer Res 2025;85(8_Suppl_1):Abstract nr 5232.

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Journal
Cancer Research
Published
2025-04-21
DOI
https://doi.org/10.1158/1538-7445.am2025-5232
Primary Topic
Cancer, Lipids, and Metabolism
Type
article
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article

Abstract 5232: Tumor-adipose microenvironment drives progression in advanced oral squamous cell carcinoma

Sumin Kang, Yu‐Sun Lee, Jiyoung Lee, Sung Weon Choi et al.
Cancer Research
Cancer, Lipids, and Metabolism
article

Abstract 5232: Tumor-adipose microenvironment drives progression in advanced oral squamous cell carcinoma

Sumin Kang, Yu‐Sun Lee, Jiyoung Lee, Sung Weon Choi, Mi Rim Lee, Sun Il Choi, Hye Won Shon, Yun Hee Kim, Guiqiong Kang
article en

Abstract

Abstract Advanced oral squamous cell carcinoma (OSCC) is an aggressive cancer with a recurrence rate of 40-60%, and lymph node metastasis (LNM) occurs in 50% of cases, serving as a critical prognostic factor. Recent evidence suggests that fatty acid oxidation (FAO) enhances cancer cell survival, invasiveness, and therapeutic resistance. OSCC's histological proximity to dense adipose tissue provides a unique opportunity for cancer cells to acquire energy from the adipose environment, underscoring the importance of elucidating the tumor-adipose interactions in OSCC progression and metastasis. In this study, we investigated the impact of the tumor-adipose microenvironment on OSCC progression, focusing on interactions between adipocytes and cancer cells. Human adipose-derived stem cells (ADSCs) were differentiated into adipocytes and co-cultured with the OSCC cell line YD10B for three weeks to induce cancer-associated adipocytes (CAAs). Co-cultured adipocytes exhibited fibroblast-like phenotypic changes, reduced expression of adipogenic differentiation markers, and increased free fatty acid release. Inflammatory cytokines (e.g., IL-6) and tumor-promoting proteins (e.g., IGFBP-2) were upregulated. YD10B cells exposed to co-cultured adipocytes showed enhanced proliferation, invasion, and epithelial-mesenchymal transition (EMT) signaling. Adipocytes and cancer cells both showed increased expression of matrix metalloproteinases (MMP-2 and MMP-9), indicating mutual reinforcement of tumor aggressiveness. Collectively, these findings indicate that adipocytes, through their interaction with OSCC cells, undergo changes to acquire a CAA-like phenotype , which support tumor progression by providing fatty acids as an energy source and promoting aggressive phenotypes, including proliferation, invasion, and LNM. Targeting tumor-adipocyte interactions could offer novel therapeutic strategies to mitigate OSCC progression and improve outcomes. Citation Format: Gyeongmin Kang, Mi Rim Lee, Sumin Kang, Yu-Sun Lee, Hye Won Shon, Jiyoung Lee, Sung Weon Choi, Sun Il Choi, Yun-Hee Kim. Tumor-adipose microenvironment drives progression in advanced oral squamous cell carcinoma [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2025; Part 1 (Regular Abstracts); 2025 Apr 25-30; Chicago, IL. Philadelphia (PA): AACR; Cancer Res 2025;85(8_Suppl_1):Abstract nr 5232.

Cancer ResearchVol. 85(8_Supplement_1)
National Cancer Center (KR)
Openalex Percentile: Top 90%
Cancer, Lipids, and Metabolism
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