Serveur d'exploration Chloroquine

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Immunomodulatory proteins FIP-gts and chloroquine induce caspase-independent cell death via autophagy for resensitizing cisplatin-resistant urothelial cancer cells.

Identifieur interne : 000D70 ( Main/Exploration ); précédent : 000D69; suivant : 000D71

Immunomodulatory proteins FIP-gts and chloroquine induce caspase-independent cell death via autophagy for resensitizing cisplatin-resistant urothelial cancer cells.

Auteurs : I-Lun Hsin [Taïwan] ; Shao-Chuan Wang [Taïwan] ; Jian-Ri Li [Taïwan] ; Tsai-Chun Ciou [Taïwan] ; Chih-Hsien Wu [Taïwan] ; Hung-Ming Wu [Taïwan] ; Jiunn-Liang Ko [Taïwan]

Source :

RBID : pubmed:27823620

Descripteurs français

English descriptors

Abstract

Chloroquine, a lysosomal inhibitor, is used for malaria, rheumatoid arthritis, and lupus erythematosus therapy. In our previous study, FIP-gts, an immunomodulatory protein from Ganoderma tsugae, inhibited cell viability in lung cancer cells and urothelial cancer cells. Urothelial carcinoma is the most common type of bladder cancer. Cisplatin resistance is an important issue in urothelial carcinoma therapy.

DOI: 10.1016/j.phymed.2016.09.003
PubMed: 27823620


Affiliations:


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Le document en format XML

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<term>Amino Acid Chloromethyl Ketones (pharmacology)</term>
<term>Antineoplastic Combined Chemotherapy Protocols (pharmacology)</term>
<term>Apoptosis (drug effects)</term>
<term>Autophagy (drug effects)</term>
<term>Caspases (metabolism)</term>
<term>Cell Cycle (drug effects)</term>
<term>Cell Line, Tumor</term>
<term>Cell Survival (drug effects)</term>
<term>Chloroquine (administration & dosage)</term>
<term>Chloroquine (pharmacology)</term>
<term>Cisplatin (pharmacology)</term>
<term>Drug Resistance, Neoplasm (drug effects)</term>
<term>Fungal Proteins (administration & dosage)</term>
<term>Fungal Proteins (pharmacology)</term>
<term>Ganoderma (chemistry)</term>
<term>Humans</term>
<term>Immunologic Factors (pharmacology)</term>
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<term>Urologic Neoplasms (drug therapy)</term>
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<term>Apoptose ()</term>
<term>Autophagie ()</term>
<term>Caspases (métabolisme)</term>
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<term>Chloroquine (administration et posologie)</term>
<term>Chloroquine (pharmacologie)</term>
<term>Cisplatine (pharmacologie)</term>
<term>Cycle cellulaire ()</term>
<term>Facteurs immunologiques (pharmacologie)</term>
<term>Ganoderma ()</term>
<term>Humains</term>
<term>Lignée cellulaire tumorale</term>
<term>Potentiel de membrane mitochondriale ()</term>
<term>Protocoles de polychimiothérapie antinéoplasique (pharmacologie)</term>
<term>Protéines fongiques (administration et posologie)</term>
<term>Protéines fongiques (pharmacologie)</term>
<term>Résistance aux médicaments antinéoplasiques ()</term>
<term>Survie cellulaire ()</term>
<term>Tumeurs urologiques (anatomopathologie)</term>
<term>Tumeurs urologiques (traitement médicamenteux)</term>
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<term>Fungal Proteins</term>
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<term>Chloroquine</term>
<term>Cisplatin</term>
<term>Fungal Proteins</term>
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<term>Protéines fongiques</term>
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<term>Autophagy</term>
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<term>Drug Resistance, Neoplasm</term>
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<term>Chloroquine</term>
<term>Cisplatine</term>
<term>Facteurs immunologiques</term>
<term>Protocoles de polychimiothérapie antinéoplasique</term>
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<term>Autophagie</term>
<term>Cycle cellulaire</term>
<term>Ganoderma</term>
<term>Humains</term>
<term>Lignée cellulaire tumorale</term>
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<front>
<div type="abstract" xml:lang="en">Chloroquine, a lysosomal inhibitor, is used for malaria, rheumatoid arthritis, and lupus erythematosus therapy. In our previous study, FIP-gts, an immunomodulatory protein from Ganoderma tsugae, inhibited cell viability in lung cancer cells and urothelial cancer cells. Urothelial carcinoma is the most common type of bladder cancer. Cisplatin resistance is an important issue in urothelial carcinoma therapy.</div>
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