CES2 Expression in Pancreatic Adenocarcinoma Is Predictive of Response to Irinotecan and Is Associated With Type 2 Diabetes

Author:

Capello Michela1,Fahrmann Johannes F.1,Rios Perez Mayrim V.2,Vykoukal Jody V.1,Irajizad Ehsan13,Tripathi Satyendra C.1,Roife David2,Bantis Leonidas E.34,Kang Ya’an2,Kundnani Deepali L.1,Xu Hanwen1,Prakash Laura R.2,Long James P.3,Katayama Hiroyuki1,Fleury Alia1,Ferri-Borgogno Sammy5,Baluya Dodge L.6,Dennison Jennifer B.1,Aguilar-Bonavides Clemente1,Casabar Julian P.1,Celiktas Muge1,Do Kim-Anh3,Fiehn Oliver7,Maitra Anirban48,Wang Huamin8,Feng Ziding3,Chiao Paul J.9,Katz Matthew H.2,Fleming Jason B.10,Hanash Samir M.1

Affiliation:

1. Department of Clinical Cancer Prevention, The University of Texas MD Anderson Cancer Center, Houston, TX

2. Department of Surgical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX

3. Department of Biostatistics, The University of Texas MD Anderson Cancer Center, Houston, TX

4. Department of Biostatistics and Data Science, University of Kansas Medical Center, Kansas City, KS

5. Department of Translational Molecular Pathology, The University of Texas MD Anderson Cancer Center, Houston, TX

6. Center for Radiation Oncology Research, The University of Texas MD Anderson Cancer Center, Houston, TX

7. University of California Davis Genome Center–Metabolomics, University of California, Davis, CA

8. Department of Pathology, The University of Texas MD Anderson Cancer Center, Houston, TX

9. Department of Molecular and Cellular Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX

10. Department of Gastrointestinal Oncology, H. Lee Moffitt Cancer Center, Tampa, FL

Abstract

PURPOSE The combination chemotherapy of fluorouracil, leucovorin, irinotecan, and oxaliplatin (FOLFIRINOX) has provided clinically meaningful improvement for pancreatic ductal adenocarcinoma (PDAC). We previously uncovered a role for the serine hydrolase carboxylesterase 2 (CES2) in mediating intratumoral activation of the prodrug irinotecan, a constituent of FOLFIRINOX. We aimed to further test the predictive value of CES2 for response to irinotecan using patient-derived xenograft (PDX) models and to elucidate the determinants of CES2 expression and response to FOLFIRINOX treatment among patients with PDAC. METHODS PDXs were engrafted subcutaneously into nude mice and treated for 4 weeks with either saline control or irinotecan. CES2 and hepatocyte nuclear factor 4 alpha (HNF4A) expression in PDAC tissues was evaluated by immunohistochemical and Western blot analysis. Kaplan-Meier and Cox regression analyses were applied to assess the association between overall survival and hemoglobin A1C (HbA1C) levels in patients who underwent neoadjuvant FOLFIRINOX treatment. RESULTS High CES2 activity in PDAC PDXs was associated with increased sensitivity to irinotecan. Integrated gene expression, proteomic analyses, and in vitro genetic experiments revealed that nuclear receptor HNF4A, which is upregulated in diabetes, is the upstream transcriptional regulator of CES2 expression. Elevated CES2 protein expression in PDAC tissues was positively associated with a history of type 2 diabetes (odds ratio, 4.84; P = .02). High HbA1C levels were associated with longer overall survival in patients who received neoadjuvant FOLFIRINOX treatment ( P = .04). CONCLUSION To our knowledge, we provide, for the first time, evidence that CES2 expression is associated with a history of type 2 diabetes in PDAC and that elevated HbA1C, by predicting tumor CES2 expression, may represent a novel marker for stratifying patients most likely to respond to FOLFIRINOX therapy.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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