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Original Article | Open Access

CLT-003 exerts anti-tumor activity in pancreatic cancer by blocking the PI3K/AKT/HIF-1α pathway

Chao Xu1,2,*Zekun Li1,*Yueying Shan1,*Chunhua She1Yanfang Yang1Tianxing Zhou1Yongjie Xie1Bo Ni1Chenyang Meng1Guangcong Shen1Boyang Fu1Guannan Sheng1Liangliang Wu1Jinlong Pei1Tiansuo Zhao1Song Gao1Hongwei Wang1Chengqi Deng3Kaiyuan Wang3Antao Chang1Chongbiao Huang1Lei Shi4Shengyu Yang5Jun Yu1Jihui Hao1 ( )Xiuchao Wang1 ( )
Pancreas Center, Tianjin Medical University Cancer Institute and Hospital, National Clinical Research Center for Cancer, State Key Laboratory of Druggability Evaluation and Systematic Translational Medicine, Tianjin Key Laboratory of Digestive Cancer, Tianjin’s Clinical Research Center for Cancer, Tianjin 300060, China
National Clinical Research Center for Cancer, Tianjin Cancer Hospital Airport Hospital, Tianjin 300060, China
Department of Anesthesiology, Tianjin Medical University Cancer Institute and Hospital, National Clinical Research Center for Cancer, Key Laboratory of Cancer Prevention and Therapy, Tianjin’s Clinical Research Center for Cancer, Tianjin 300060, China
Department of Biochemistry and Molecular Biology, School of Basic Medical Sciences, Tianjin Medical University, Tianjin 300070, China
Department of Cellular and Molecular Physiology, Penn State College of Medicine, Hershey, Pennsylvania 17033, USA

*These authors contributed equally to this work.

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Abstract

Objective

CLT-003 is a novel phenylphthalimide derivative encapsulated in poly (lactate-glycolic acid) copolymer nanoparticles using nanotechnology techniques. CLT-003 possesses anti-angiogenetic and antitumor activities. Nevertheless, the role and molecular mechanism underlying CLT-003 in pancreatic cancer remain to be elucidated.

Methods

Cell proliferation and apoptosis were detected using CCK-8, real-time cell analysis (RTCA), EdU, and flow cytometric assays. Cellular mobility and invasive capacity were detected using wound-healing, Transwell, and cell motility assays. Tumor growth and metastasis were determined using the mouse subcutaneous and pancreatic cancer orthotopic liver metastasis models. The antitumor effects of CLT-003 were evaluated using patient-derived organoid (PDO) and patient-derived xenograft (PDX) models.

Results

CLT-003 significantly inhibited cellular proliferation, enhanced cellular apoptosis, and attenuated cellular invasion and migration of pancreatic cancer cells. Mechanistically, CLT-003 suppressed the translation of HIF-1α by inhibiting the PI3K/AKT/mTOR signaling pathway. In the mouse tumor models, CLT-003 significantly inhibited the growth and metastasis of pancreatic tumors. Moreover, the PDO and PDX models showed increased sensitivity to CLT-003 in pancreatic cancer with high HIF-1α expression compared to pancreatic cancer with low HIF-1α expression.

Conclusions

This study delineated the role and molecular mechanism of CLT-003 action in impeding the progression of pancreatic cancer and indicated its robust potential for the treatment of pancreatic cancer.

Electronic Supplementary Material

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Cancer Biology & Medicine
Pages 1558-1577

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Cite this article:
Xu C, Li Z, Shan Y, et al. CLT-003 exerts anti-tumor activity in pancreatic cancer by blocking the PI3K/AKT/HIF-1α pathway. Cancer Biology & Medicine, 2025, 22(12): 1558-1577. https://doi.org/10.20892/j.issn.2095-3941.2025.0058

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Received: 10 February 2025
Accepted: 24 July 2025
Published: 30 September 2025
©2025 The Authors.

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