Tuning Push-Pull Electronic Effects of AIEgens to Boost the Theranostic Efficacy for Colon Cancer.
Hai-Tao FengShaomin ZouMing ChenFeng XiongMong-Hong LeeLekun FangBen-Zhong TangPublished in: Journal of the American Chemical Society (2020)
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-OM, 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.
Keyphrases
- cell cycle
- cancer therapy
- single cell
- cell proliferation
- photodynamic therapy
- gene expression
- fluorescence imaging
- high resolution
- drug delivery
- cell therapy
- emergency department
- quantum dots
- mesenchymal stem cells
- papillary thyroid
- solar cells
- combination therapy
- cardiovascular disease
- living cells
- squamous cell
- genome wide identification
- mass spectrometry
- bone marrow
- genome wide analysis
- copy number
- molecularly imprinted
- simultaneous determination