An Isoquinolin‐1(2H)‐Imine Derivative Induces Cell Death via Generation of Reactive Oxygen Species and Activation of JNK in Human A549 Cancer Cells. Issue 12 (31st May 2017)
- Record Type:
- Journal Article
- Title:
- An Isoquinolin‐1(2H)‐Imine Derivative Induces Cell Death via Generation of Reactive Oxygen Species and Activation of JNK in Human A549 Cancer Cells. Issue 12 (31st May 2017)
- Main Title:
- An Isoquinolin‐1(2H)‐Imine Derivative Induces Cell Death via Generation of Reactive Oxygen Species and Activation of JNK in Human A549 Cancer Cells
- Authors:
- Liu, Jing
Liu, Tongyang
Mou, Hanchuan
Jia, Shuting
Huang, Chao
Yan, Shengjiao
Lin, Jun
Luo, Ying
Zhang, Jihong - Abstract:
- ABSTRACT: Compound 11‐benzoyl‐10‐chloro‐7, 9‐difluoro‐6‐imino‐2, 3, 4, 6‐tetrahydro‐1H‐pyrimido[1, 2‐b]isoquinoline‐8‐carbonitrile (HC6h) is a novel polyhalo 1, 3‐diazaheterocycle fused isoquinolin‐1(2H)‐imines derivative, which displays good anticancer activity and low toxicity in vivo. However, the underlying anticancer mechanisms have not previously been identified. The proliferation of A549 was assessed by MTT assay. The reactive oxygen species (ROS) level was assessed in A549 with a H2 DCFDA probe. Mitochondrial membrane potential was measured using the JC‐1 staining. Apoptosis were measured by annexin‐V/PI assay and autophagy by acridine orange staining and GFP‐LC3 fluorescence assay. The expression of autophagic and apoptotic proteins was determined by Western blot. The compound HC6h increased accumulation of vesicles, acridine orange‐stained cells and LC3‐II in A549 cells. Inhibition of compound HC6h‐induced autophagy by bafilomycin A1 increased apoptosis. Compound HC6h enhanced activation of caspase‐3, caspase‐9 and PARP cleavage in A549 cells. Compound HC6h leads to the rapid generation of intracellular ROS. Moreover, compound HC6h induced phosphorylation of JNK and was conferred by the increased ROS levels. Furthermore, down‐regulation of JNK attenuated autophagic and apoptotic effect in response to HC6h. The induction of ROS upon HC6h treatment leads to the activation of JNK that mediates autophagy and apoptosis in human A549 cancer cells. J. Cell. Biochem. 118:ABSTRACT: Compound 11‐benzoyl‐10‐chloro‐7, 9‐difluoro‐6‐imino‐2, 3, 4, 6‐tetrahydro‐1H‐pyrimido[1, 2‐b]isoquinoline‐8‐carbonitrile (HC6h) is a novel polyhalo 1, 3‐diazaheterocycle fused isoquinolin‐1(2H)‐imines derivative, which displays good anticancer activity and low toxicity in vivo. However, the underlying anticancer mechanisms have not previously been identified. The proliferation of A549 was assessed by MTT assay. The reactive oxygen species (ROS) level was assessed in A549 with a H2 DCFDA probe. Mitochondrial membrane potential was measured using the JC‐1 staining. Apoptosis were measured by annexin‐V/PI assay and autophagy by acridine orange staining and GFP‐LC3 fluorescence assay. The expression of autophagic and apoptotic proteins was determined by Western blot. The compound HC6h increased accumulation of vesicles, acridine orange‐stained cells and LC3‐II in A549 cells. Inhibition of compound HC6h‐induced autophagy by bafilomycin A1 increased apoptosis. Compound HC6h enhanced activation of caspase‐3, caspase‐9 and PARP cleavage in A549 cells. Compound HC6h leads to the rapid generation of intracellular ROS. Moreover, compound HC6h induced phosphorylation of JNK and was conferred by the increased ROS levels. Furthermore, down‐regulation of JNK attenuated autophagic and apoptotic effect in response to HC6h. The induction of ROS upon HC6h treatment leads to the activation of JNK that mediates autophagy and apoptosis in human A549 cancer cells. J. Cell. Biochem. 118: 4394–4403, 2017. © 2017 Wiley Periodicals, Inc. Abstract : HC6h induced apoptosis and autophagy via the ROS‐dependent JNK signaling pathway in A549 cells. Cancer cells activated incomplete autophagy with HC6h treatment and inhibition of autophagy by autophagy inhibitor significantly augmented cell death on HC6h treatment. … (more)
- Is Part Of:
- Journal of cellular biochemistry. Volume 118:Issue 12(2017)
- Journal:
- Journal of cellular biochemistry
- Issue:
- Volume 118:Issue 12(2017)
- Issue Display:
- Volume 118, Issue 12 (2017)
- Year:
- 2017
- Volume:
- 118
- Issue:
- 12
- Issue Sort Value:
- 2017-0118-0012-0000
- Page Start:
- 4394
- Page End:
- 4403
- Publication Date:
- 2017-05-31
- Subjects:
- ISOQUINOLIN -- AUTOPHAGY -- APOPTOSIS -- ROS
Cytochemistry -- Periodicals
572 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1097-4644 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/jcb.26093 ↗
- Languages:
- English
- ISSNs:
- 0730-2312
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4955.010000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 23483.xml