Regulating Twisted Skeleton to Construct Organ‐Specific Perylene for Intensive Cancer Chemotherapy

• Published in: Angewandte Chemie International Edition Vol. 60; no. 29; pp. 16215 - 16223
• Main Authors: Liu, Zhonghua, Wang, Xuejuan, Chen, Qing, Ma, Feiyan, Huang, Yongwei, Gao, Yijian, Deng, Qingyuan, Qiao, Zeng‐Ying, Xing, Xiaoyi, Zhu, Jianling, Lu, Feng, Wang, Hao
• Format: Journal Article
• Language: English
• Published: WEINHEIM Wiley 12.07.2021; Wiley Subscription Services, Inc
• Edition: International ed. in English
• Subjects: Adenosine triphosphate; Animals; Antineoplastic Agents - chemistry; Antineoplastic Agents - pharmacology; Antineoplastic Agents - therapeutic use; Apoptosis; Apoptosis - drug effects; ATP; Autophagy; Calcium; Cell Line, Tumor; Cell Proliferation - drug effects; Chemistry; Chemistry, Multidisciplinary; Chemotherapy; Drug development; Drug Screening Assays, Antitumor; Endoplasmic reticulum; fluorescence image; Humans; Hydrogen peroxide; Lung cancer; Lung Neoplasms - drug therapy; Lung Neoplasms - metabolism; Lung Neoplasms - pathology; Metastases; Mice; Mitochondria; molecular mechanism; perylene; Perylene - analogs & derivatives; Perylene - chemistry; Perylene - pharmacology; Phagocytosis; Pharmaceuticals; Physical Sciences; Science & Technology; Side effects; twisted skeleton; Xenografts; CELLS; APOPTOSIS; fluorescence image; ER-STRESS; MITOCHONDRIA; MECHANISMS; chemotherapy; DELIVERY; perylene; LUNG-CANCER; molecular mechanism; IMPACT; twisted skeleton; AGENTS; PROBE
• ISSN: 1433-7851; 1521-3773; 1521-3773
• DOI: 10.1002/anie.202105607

The systemic use of pharmaceutical drugs for cancer patients is a compromise between desirable therapy and side effects because of the intrinsic shortage of organ‐specific pharmaceutical drug. Design and construction of pharmaceutical drug to achieve the organ‐specific delivery is thus desperately desirable. We herein regulate perylene skeleton to effect organ‐specificity and present an example of lung‐specific distribution on the basis of bay‐twisted PDIC‐NC. We further demonstrate that PDIC‐NC can target into mitochondria to act as cellular respiration inhibitor, inducing insufficient production of adenosine triphosphate, promoting endogenous H2O2 and .OH burst, elevating calcium overload, efficiently triggering the synergistic apoptosis, autophagy and endoplasmic reticulum stress of lung cancer cells. The antitumor performance of PDIC‐NC is verified on in vivo xenografted, metastasis and orthotopic lung cancer, presenting overwhelming evidences for potentially clinical application. This study contributes a proof‐of‐concept demonstration of twisted perylene to well attain lung‐specific distribution, and meanwhile achieves intensive lung cancer chemotherapy. Herein we modulate the perylene skeleton to effect organ‐specificity and present an example of lung‐specific distribution on the basis of a twisted perylene PDIC‐NC. The in vitro and in vivo biological functions of PDIC‐NC are demonstrated and its molecular mechanism for the inhibiting activity on tumour cells is revealed.