Chun‐Li Su

ORCID: 0000-0001-7617-2077
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About
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Research Areas
  • Autophagy in Disease and Therapy
  • Cancer-related Molecular Pathways
  • Plant-derived Lignans Synthesis and Bioactivity
  • Microtubule and mitosis dynamics
  • Cell death mechanisms and regulation
  • Curcumin's Biomedical Applications
  • Cancer, Lipids, and Metabolism
  • NF-κB Signaling Pathways
  • Natural product bioactivities and synthesis
  • Bioactive Compounds and Antitumor Agents
  • Genomics, phytochemicals, and oxidative stress
  • Ferroptosis and cancer prognosis
  • Sirtuins and Resveratrol in Medicine
  • Histone Deacetylase Inhibitors Research
  • Cancer, Hypoxia, and Metabolism
  • Calcium signaling and nucleotide metabolism
  • Epigenetics and DNA Methylation
  • Synthesis of Indole Derivatives
  • Metabolism and Genetic Disorders
  • Synthesis and bioactivity of alkaloids
  • Ginseng Biological Effects and Applications
  • Animal Nutrition and Physiology
  • Cancer-related molecular mechanisms research
  • Drug-Induced Hepatotoxicity and Protection
  • Endoplasmic Reticulum Stress and Disease

National Taiwan Normal University
2015-2025

Cornell University
1994-2016

New York State College of Veterinary Medicine
2016

Chang Jung Christian University
2005-2012

National Cheng Kung University
2008

Kaohsiung Medical University
2008

National Institutes of Health
2003

National Institute of Diabetes and Digestive and Kidney Diseases
2003

National Yang Ming Chiao Tung University
2002-2003

Thioridazine (THD) is a common phenothiazine antipsychotic drug reported to suppress growth in several types of cancer cells. We previously showed that THD acts as an antiglioblastoma and anticancer stem-like cell agent. However, the signaling pathway underlying autophagy apoptosis induction remains unclear. treatment significantly induced with upregulated AMPK activity engendered death increased sub-G1 glioblastoma multiform (GBM) lines. Notably, through whole gene expression screening...

10.3390/ijms20030473 article EN International Journal of Molecular Sciences 2019-01-22

Ferroptosis, a recently discovered form of iron-dependent cell death, requires an increased level lipid-reactive oxygen species (ROS). Ferritinophagy, ferritin degradation pathway, depends on selective autophagic cargo receptor (NCOA4). By screening various types natural compounds, formosanin C (FC) was identified as novel ferroptosis inducer, characterized by attenuations FC-induced viability inhibition and lipid ROS formation in the presence inhibitor. FC also induced flux, evidenced...

10.3390/antiox9080682 article EN cc-by Antioxidants 2020-07-29

Dysfunction of degradation machineries causes cancers, including hepatocellular carcinoma (HCC). Overexpression cyclin D1 in HCC has been reported. We previously reported that autophagy preferentially recruits and degrades the oncogenic microRNA (miR)‐224 to prevent HCC. Therefore, present study, we attempted clarify whether is another factor selectively regulated by tumorigenesis. Initially, found an inverse correlation between low autophagic activity high expression tumors 147 patients...

10.1002/hep.29781 article EN cc-by-nc-nd Hepatology 2018-01-12

Lipolysis in adipocytes governs the release of fatty acids for supply energy to various tissues body. This reaction is mediated by hormone-sensitive lipase (HSL), a cytosolic enzyme, and perilipin, which coats lipid droplet surface adipocytes. Both HSL perilipin are substrates polyphosphorylation protein kinase A (PKA), phosphorylation required induce translocate from cytosol droplet, critical step lipolytic (Sztalryd C., Xu, G., Dorward, H., Tansey, J. T., Contreras, J.A, Kimmel, A. R.,...

10.1074/jbc.m301809200 article EN cc-by Journal of Biological Chemistry 2003-10-01

Curcumin, an active compound in turmeric and curry, has been proven to induce tumor apoptosis inhibit proliferation, invasion, angiogenesis, metastasis via modulating numerous targets various types of cancer cells. Aurora A is a mitosis-related serine-threonine kinase plays important roles diverse human cancers. However, the effect curcumin on not reported. In this study, promoter activity mRNA expression were inhibited curcumin-treated bladder T24 cells, suggesting that regulated at...

10.1124/mol.111.072512 article EN Molecular Pharmacology 2011-07-14

Targeting ferritin via autophagy (ferritinophagy) to induce ferroptosis, an iron- and reactive oxygen species (ROS)-dependent cell death, provides novel strategies for cancer therapy. Using a ferroptosis-specific inhibitor iron chelator, the vulnerability of triple-negative breast (TNBC) MDA-MB-231 cells ferroptosis was identified compared that luminal A MCF-7 cells. Saponin formosanin C (FC) revealed as potent inducer characterized by superior induction in cytosolic lipid ROS formation well...

10.3390/antiox11020298 article EN cc-by Antioxidants 2022-01-31

The E. coli strains harboring the polyketide synthase (pks) island encode genotoxin colibactin, a secondary metabolite reported to have severe implications for human health and progression of colorectal cancer. present study involves whole-genome-wide comparison phylogenetic analysis pks isolates gain insight into distribution evolution these organisms. Fifteen isolated from patients with ulcerative colitis (UC) were sequenced, 13 which harbored islands. In addition, 2,654 genomes public...

10.1186/s12864-024-11198-x article EN cc-by-nc-nd BMC Genomics 2025-01-08

The natural product justicidin A, an arylnaphthalide lignan isolated from Justicia procumbens, significantly inhibited the growth of human colorectal cancer cells HT-29 and HCT 116 at day 6 post-treatment. Further study revealed that A-treated died apoptosis. Justicidin A treatment caused DNA fragmentation increase in phosphatidylserine exposure cells. number sub-G1 phase was also increased upon treatment. Caspase-9 but not caspase-8 activated, suggesting damaged mitochondria. mitochondrial...

10.1093/carcin/bgi133 article EN Carcinogenesis 2005-05-19

Our previous reports showed that justicidin A (JA), a novel and pure arylnaphthalide lignan isolated from Justicia procumbens , induces apoptosis of human colorectal cancer cells hepatocellular carcinoma cells, leading to the suppression both tumor cell growth in NOD‐SCID mice. Here, we reveal JA autophagy HT‐29 by conversion autophagic marker LC3‐I LC3‐II. Furthermore, LC3 puncta vesicle formation, SQSTM1/p62 were observed. Administration inhibitor (bafilomycin A1 chloroquine) transfection...

10.1002/jcp.24825 article EN Journal of Cellular Physiology 2014-09-12

Abstract Formosanin C (FC) is a natural compound extracted from Paris formosana Hayata with anticancer activity. FC induces both autophagy and apoptosis in human lung cancer cells. FC‐induced depolarization of mitochondrial membrane potential (MMP) may trigger mitophagy. In this study, we clarified the effect on autophagy, mitophagy, role FC‐related cell death motility. We found caused continuous increase LC3 II (representing autophagosomes) 24 to 72 h without degradation after treatment...

10.1002/kjm2.12658 article EN cc-by-nc-nd The Kaohsiung Journal of Medical Sciences 2023-03-03

Three experiments were conducted to determine the effect of excess dietary protein on threonine requirement broiler chicks 14 d age (Experiments 1 and 2) from 16 28 (Experiment 3). Two levels used in Experiments 2:20% CP a threonine-limiting basal diet containing wheat, peanut meal, selected amino acids 25% same supplemented with mixture lacking threonine. A based corn, soybean was also included Experiment 2. The determined using single level (20%) 3. Threonine requirements estimated by...

10.3382/ps.0730670 article EN cc-by-nc-nd Poultry Science 1994-05-01

Formosanin C is a pure compound isolated from Paris formosana Hayata (Liliaceae). The antitumor efficacy of formosanin has been observed in cultured cells and animal systems. However, the molecular mechanisms remain unknown. results present study indicate that induced apoptosis HT-29 characterized by exposure phosphatidylserine, accumulation at sub-G(1) phase, fragmentation DNA, change nuclear morphology time- dose-related manner. apoptotic signaling cascades may proceed via proteolytic...

10.1111/j.1349-7006.2008.01057.x article EN other-oa Cancer Science 2008-12-19

Justicia procumbens is a traditional Taiwanese herbal remedy used to treat fever, pain, and cancer. Justicidin A, isolated from , has been reported suppress in vitro growth of several tumor cell lines as well hepatoma cells. In this study, justicidin A activated caspase‐8 increase tBid, disrupted mitochondrial membrane potential (Δ ψ m ), caused the release cytochrome c Smac/DIABLO Hep 3B G2 also reduced Bcl‐x L increased Bax Bak mitochondria. Caspase‐8 inhibitor (Z‐IETD) attenuated...

10.1016/j.febslet.2006.04.085 article EN FEBS Letters 2006-05-04

Drug resistance and tumor recurrence are major obstacles in treating lung cancer patients. Accumulating evidence considers stem cells (CSCs) as the contributor to these clinical challenges. Agents that can target CSCs could potentially provide a more effective treatment than traditional chemotherapy. Here, we utilized side-population (SP) method isolate from A549 PC-9 cell lines. Subsequently, high throughput platform, connectivity maps (CMAPs), was used identify potential anti-CSC agents....

10.1155/2013/910451 article EN Evidence-based Complementary and Alternative Medicine 2013-01-01

Curcumin, an active natural compound in turmeric and curry, has been reported to exhibit anti-cancer effect. Cisplatin, carboplatin oxaliplatin are used treat various types of cancers. However, acquired resistance toxicities observed. Here, the addition curcumin significantly increased cytotoxicity drugs on human colorectal cancer HT-29 cells, producing synergistic (cisplatin carboplatin) additivity (oxaliplatin) effects. Treatments combination with resulted a induction apoptosis occurrence...

10.3109/09637486.2013.871694 article EN International Journal of Food Sciences and Nutrition 2014-01-20

Analysis of various public databases revealed that HRAS gene mutation frequency and mRNA expression are higher in bladder urothelial carcinoma. Further analysis the roles oncogenic HRAS, autophagy, cell senescence signaling cancer cells sensitized to anticancer drug cisplatin using phytochemical pterostilbene. A T24 line with was chosen for further experiments. Indeed, coadministration pterostilbene increased stronger cytotoxicity on compared wild-type E7 cells, which paralleled by neither...

10.3390/cancers12102869 article EN Cancers 2020-10-06

Abstract Background Despite advances in treatment, patients with refractory colorectal cancer (CRC) still have poor long-term survival, so there is a need for more effective therapeutic options. Methods To evaluate the HDAC8 inhibition efficacy as CRC we examined effects of various inhibitors (HDAC8i), including BMX (NBM-T-L-BMX-OS01) combination temozolomide (TMZ) or other standard drugs on p53 mutated HT29 cells, well wild-type HCT116 and RKO cells. Results We showed that HDAC8i TMZ...

10.1186/s12964-022-01007-x article EN cc-by Cell Communication and Signaling 2022-12-27

Bufotalin is one of the bufadienolides isolated from Formosan Ch'an Su, which made skin and parotid glands toads. Ingestion toad venom results in severe morbidity high mortality. Although Su clinically toxic, it has been used as an important traditional Chinese medicine for heart failure pains. In this study, bufotalin-induced apoptosis human hepatocellular carcinoma Hep 3B cells was investigated. The indicate that externalization phosphatidylserine, accumulation sub-G1 cells, fragmentation...

10.1021/jf802769g article EN Journal of Agricultural and Food Chemistry 2008-12-04

Coronavirus disease 2019 (COVID-19) remains a threat with the emergence of new variants, especially Delta and Omicron, without specific effective therapeutic drugs. The infection causes dysregulation immune system cytokine storm that eventually leads to fatal acute respiratory distress syndrome (ARDS) further irreversible pulmonary fibrosis. Therefore, promising way inhibit is disrupt binding fusion between viral spike host ACE2 receptor. A transcriptome-based drug screening platform has...

10.3389/fphar.2022.905197 article EN cc-by Frontiers in Pharmacology 2022-07-04
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