A Super-Assembled Synergistically Nanoplatform AP@ZIF-8Pt for Hepatocarcinoma Therapy

Zhenzhen Luo,1,* Dunhuang Wang,2,* Lie Lin,2 Rui Zhou,2 Yuanyuan Su,2 Zongkai Zhang,2 Jing Hu,2 Yaqing Dai,2 Jingjing Wu,2 Xiaoyan Huang,2 Yufei Zhou,2 Liuyun Gong2 1Shenzhen Cancer Hospital, Chinese Academy of Medical Sciences, Shenzhen, Guangdong, 518000, People’s Republic of China; 2Department of Radiation Oncology, Xiamen Cancer Quality Control Center, Xiamen Cancer Center, Xiamen Key Laboratory of Radiation Oncology, The First Affiliated Hospital of Xiamen University, School of Medicine, Xiamen University, Xiamen, Fujian, 361003, People’s Republic of China*These authors contributed equally to this workCorrespondence: Liuyun Gong, Email [email protected] Yufei Zhou, Email [email protected]: Intensive cancer treatment with nanoplatform is widely exploited in the clinic, the emerging nanomedicine offers an unparalleled opportunity for encapsulating potential antitumor drugs in a nano-carrier. Apoptin (AP), a coding protein of VP3 gene, stem from the chicken anemia virus (CAV), can be activated in malignant cells selectively and prevents the dividing cancer cells from repairing their DNA lesions, thereby forcing them to undergo apoptosis. Herein, a three-step intelligent biodegradable drug delivery nanoplatform was designed.Methods: First, a hollow ZIF-8 was synthesized, embedded with platinum nanoparticle to form ZIF-8Pt, and then loaded with AP, and lastly formed AP@ZIF-8Pt, which possess pH-responsive drug release and cancer-targeted ability.Results: As expected, both in vitro and in vivo experiment demonstrated that AP@ZIF-8Pt performed treatment effects in hepatocarcinoma through relieving tumor-hypoxic microenvironment, inhibiting cell proliferation and promoting cell apoptosis. Further transcriptomic analysis showed that the specific mechanism of the AP@ZIF-8Pt was thermogenesis, signaling pathways regulating pluripotency of stem cells, ribosome, prion disease and PI3K-Akt signaling pathway.Discussion: This work highlights a new strategy for liver cancer treatment and provides a reference for treating malignant tumors. Keywords: AP@ZIF-8Pt, tumor-hypoxic microenvironment, apoptosis, PI3K-Akt signaling pathway

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SHILAP Revista de lepidopterología
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2025-05-01
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Latin American and Latino Studies
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article

A Super-Assembled Synergistically Nanoplatform AP@ZIF-8Pt for Hepatocarcinoma Therapy

SHILAP Revista de lepidopterología
Latin American and Latino Studies
article

A Super-Assembled Synergistically Nanoplatform AP@ZIF-8Pt for Hepatocarcinoma Therapy

article en

Abstract

Zhenzhen Luo,1,* Dunhuang Wang,2,* Lie Lin,2 Rui Zhou,2 Yuanyuan Su,2 Zongkai Zhang,2 Jing Hu,2 Yaqing Dai,2 Jingjing Wu,2 Xiaoyan Huang,2 Yufei Zhou,2 Liuyun Gong2 1Shenzhen Cancer Hospital, Chinese Academy of Medical Sciences, Shenzhen, Guangdong, 518000, People’s Republic of China; 2Department of Radiation Oncology, Xiamen Cancer Quality Control Center, Xiamen Cancer Center, Xiamen Key Laboratory of Radiation Oncology, The First Affiliated Hospital of Xiamen University, School of Medicine, Xiamen University, Xiamen, Fujian, 361003, People’s Republic of China*These authors contributed equally to this workCorrespondence: Liuyun Gong, Email [email protected] Yufei Zhou, Email [email protected]: Intensive cancer treatment with nanoplatform is widely exploited in the clinic, the emerging nanomedicine offers an unparalleled opportunity for encapsulating potential antitumor drugs in a nano-carrier. Apoptin (AP), a coding protein of VP3 gene, stem from the chicken anemia virus (CAV), can be activated in malignant cells selectively and prevents the dividing cancer cells from repairing their DNA lesions, thereby forcing them to undergo apoptosis. Herein, a three-step intelligent biodegradable drug delivery nanoplatform was designed.Methods: First, a hollow ZIF-8 was synthesized, embedded with platinum nanoparticle to form ZIF-8Pt, and then loaded with AP, and lastly formed AP@ZIF-8Pt, which possess pH-responsive drug release and cancer-targeted ability.Results: As expected, both in vitro and in vivo experiment demonstrated that AP@ZIF-8Pt performed treatment effects in hepatocarcinoma through relieving tumor-hypoxic microenvironment, inhibiting cell proliferation and promoting cell apoptosis. Further transcriptomic analysis showed that the specific mechanism of the AP@ZIF-8Pt was thermogenesis, signaling pathways regulating pluripotency of stem cells, ribosome, prion disease and PI3K-Akt signaling pathway.Discussion: This work highlights a new strategy for liver cancer treatment and provides a reference for treating malignant tumors. Keywords: AP@ZIF-8Pt, tumor-hypoxic microenvironment, apoptosis, PI3K-Akt signaling pathway

SHILAP Revista de lepidopterología
Texas Oncology (US), Radiation Oncology Associates (US), Molecular Oncology (United States) (US), Union Hospital (US)
Openalex Percentile: Top 41%
Latin American and Latino Studies
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