4.8 Article

Tuning Push-Pull Electronic Effects of AIEgens to Boost the Theranostic Efficacy for Colon Cancer

Journal

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 142, Issue 26, Pages 11442-11450

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/jacs.0c02434

Keywords

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Funding

  1. National Nature Science Foundation of China [21788102, 21805002, 81773098, 81630072, 81602429]
  2. University Grants Committee of Hong Kong [AoE/P-03/08]
  3. Research Grants Council of Hong Kong [16308016, 16305518, C6009-17G]
  4. Innovation and Technology Commission [ITC-CNERC14SC01, ITS/254/17]
  5. Natural Science Basic Research Plan in Shaanxi Province of China [2018JQ2046]
  6. Youths Talents Support Program of Shaanxi Association for Science and Technology [20190610]
  7. Pearl River S&T Nova Program of Guangzhou [201806010036]
  8. Guangdong Special Young Talent Plan of Scientific and Technological Innovation [2019TQ05Y510]
  9. Guangdong International Joint Research Program [906287430073]
  10. National Key Clinical Discipline, Shaanxi Provincial Key Laboratory Project [13JS006]

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Colon cancer is one of the most common cancers with high mortality in humans. Early diagnosis and treatment of colon cancer is of great significance for cancer therapy. Numerous theranostic agents have been developed to detect and kill cancer cells. However, few reports have focused on how these agents control and affect the gene expression of cancer cells in vivo. Herein, three pyridinium-functionalized tetraphenylethylene derivatives, namely, TPE-OK TPE-H, and TPE-NO2, with electron-donating and electron-withdrawing groups were facilely synthesized as theranostic agents for cell imaging and anticolon cancer therapy. Among these AIE luminogens (AIEgens), TPE-OM with donor and acceptor structure showed the best treatment efficacy for colon cancer through systematic biological evaluation and comparison. Both in vitro cell imaging and in vivo tumor treatment experiments demonstrated that TPE-OM can be utilized as an efficient theranostic agent to diagnose and kill colon cancer cells. Flow cytometric analysis revealed that the cell cycle process was disturbed by TPE-OM in colon cancer cells. Deep insight into the gene level revealed that the expressions of cell-cycle-promoting genes was inhibited upon addition of TPE-OM. This study may open a new venue for unraveling the mechanisms of cancer metastasis.

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