Abstract 1048: Smad deficiency impacts chemotherapeutic responses through alterations in immuno-stromal microenvironment of pancreatic adenocarcinoma

Abstract Background: Pancreatic adenocarcinoma (PDAC) is a devastating cancer with a dismal prognosis. Preoperative chemotherapy (PreOP_CT) has reshaped the treatment paradigm. However, factors influencing therapeutic responses and immune/stromal alterations have not been established. Smad family exerts pivotal biological actions through transforming growth factor-β (TGFβ) axis and affects tumor microenvironment (TME), yet the correlation with therapeutic responses has not been fully explored. Methods: We explored a prospective cohort of patients with resectable PDAC who received PreOP_CT. Genomic aberrations of the Smad family in the TGFβ axis were assessed and compared for clinical outcomes. Single-cell RNA sequencing delineated the immuno-stromal alterations in Smad-deficient vs. -proficient tumors. Results: Fifteen of 106 patients had Smad-deficient tumors and showed reduced tumor regression, higher metastatic progression and adverse survival as compared with -proficient ones. SMAD4 or TGFBR2/3 mutations were observed in Smad-deficient tumors. Smad deficiency correlated with different enrichments of tumor-infiltrating immune cells (TIMCs) and cancer-associated fibroblasts (CAFs). Collectively, inflammatory and antigen-presenting CAFs were distinctive in the deficient tumors and presented with immune evasive actions. Conclusion: Smad deficiency influences therapeutic and surgical outcomes in PreOP_CT-treated PDAC. The Smad family potentially affects TIMCs and CAFs, potentiating an immune evasive and profibrotic TME. The results provide insight into a putative biomarker for PreOP therapies in PDAC. Citation Format: Chih Chieh Yen, Ying Jui Chao, Ping Jui Su, Ting Kai Liao, Wei Hsun Lu, Zhe Wei Hsu, Chien Jui Huang, I Ting Liu, Wen Yen Huang, Yan Shen Shan, Chia Jui Yen. Smad deficiency impacts chemotherapeutic responses through alterations in immuno-stromal microenvironment of pancreatic adenocarcinoma [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 1048.

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Journal
Cancer Research
Published
2026-04-03
DOI
https://doi.org/10.1158/1538-7445.am2026-1048
Primary Topic
TGF-β signaling in diseases
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article
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article

Abstract 1048: Smad deficiency impacts chemotherapeutic responses through alterations in immuno-stromal microenvironment of pancreatic adenocarcinoma

Ting‐Kai Liao, Chun‐Yao Huang, Ying Jui Chao, Ping Su et al.
Cancer Research
TGF-β signaling in diseases
article

Abstract 1048: Smad deficiency impacts chemotherapeutic responses through alterations in immuno-stromal microenvironment of pancreatic adenocarcinoma

Ting‐Kai Liao, Chun‐Yao Huang, Ying Jui Chao, Ping Su, Chih Chieh Yen, Wen Yen Huang, Chia Jui Yen, Yan Shen Shan (6449237), Wei Hsun Lu, Zhe Wei Hsu, I Ting Liu
article en

Abstract

Abstract Background: Pancreatic adenocarcinoma (PDAC) is a devastating cancer with a dismal prognosis. Preoperative chemotherapy (PreOP_CT) has reshaped the treatment paradigm. However, factors influencing therapeutic responses and immune/stromal alterations have not been established. Smad family exerts pivotal biological actions through transforming growth factor-β (TGFβ) axis and affects tumor microenvironment (TME), yet the correlation with therapeutic responses has not been fully explored. Methods: We explored a prospective cohort of patients with resectable PDAC who received PreOP_CT. Genomic aberrations of the Smad family in the TGFβ axis were assessed and compared for clinical outcomes. Single-cell RNA sequencing delineated the immuno-stromal alterations in Smad-deficient vs. -proficient tumors. Results: Fifteen of 106 patients had Smad-deficient tumors and showed reduced tumor regression, higher metastatic progression and adverse survival as compared with -proficient ones. SMAD4 or TGFBR2/3 mutations were observed in Smad-deficient tumors. Smad deficiency correlated with different enrichments of tumor-infiltrating immune cells (TIMCs) and cancer-associated fibroblasts (CAFs). Collectively, inflammatory and antigen-presenting CAFs were distinctive in the deficient tumors and presented with immune evasive actions. Conclusion: Smad deficiency influences therapeutic and surgical outcomes in PreOP_CT-treated PDAC. The Smad family potentially affects TIMCs and CAFs, potentiating an immune evasive and profibrotic TME. The results provide insight into a putative biomarker for PreOP therapies in PDAC. Citation Format: Chih Chieh Yen, Ying Jui Chao, Ping Jui Su, Ting Kai Liao, Wei Hsun Lu, Zhe Wei Hsu, Chien Jui Huang, I Ting Liu, Wen Yen Huang, Yan Shen Shan, Chia Jui Yen. Smad deficiency impacts chemotherapeutic responses through alterations in immuno-stromal microenvironment of pancreatic adenocarcinoma [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 1048.

Cancer ResearchVol. 86(7_Supplement)
National Cheng Kung University Hospital (TW), National Cheng Kung University (TW)
Good health and well-being
Openalex Percentile: Top 29%
TGF-β signaling in diseases
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