Relations between approved platinum drugs and non-coding RNAs in mesothelioma

Autor: Bernhard Biersack
Jazyk: angličtina
Rok vydání: 2018
Předmět:
Mesothelioma
0301 basic medicine
Bcl-2
B-cell lymphoma 2

endocrine system diseases
DHA
docosahexaenoic acid

Biochemistry
Carboplatin
chemistry.chemical_compound
0302 clinical medicine
RA
retinoic acid

TSA
trichostatin A

MPM
malignant pleural mesothelioma

Medicine
HOTAIR
HOX transcript antisense RNA

SFN
sulforaphane

media_common
MALAT1
metastasis-associated lung adenocarcinoma transcript 1

DIM
3
3′-diindolylmethane

EGCG
epigallocatechin-3-gallate

MRP1
multidrug resistance protein 1

ABC
ATP-binding cassette

MicroRNA
Long non-coding RNA
Pemetrexed
DMPM
diffuse malignant peritoneal mesothelioma

030220 oncology & carcinogenesis
SAHA
suberoylanilide hydroxamic acid

I3C
indole-3-carbinol

PEG
polyethylene glycole

EMT
epithelial-mesenchymal transition

medicine.drug
Drug
lcsh:QH426-470
PEITC
phenethylisothiocyanate

NaB
sodium butyrate

media_common.quotation_subject
AKI
acute kidney injury

Anticancer drugs
AKBA
3-acetyl-11-keto-β-boswellic acid

Article
TNBC
triple-negative breast cancer

03 medical and health sciences
NSCLC
non-small cell lung cancer

microRNA
PDCD4
programmed cell death 4

Genetics
Molecular Biology
neoplasms
DADS
diallyl sulfide

CAF
cancer-associated fibroblast

Cisplatin
business.industry
CBDCA
cyclobutane-1
1-dicarboxylate

Biochemistry (medical)
medicine.disease
PTEN
phosphatase and tensin homolog

Gemcitabine
respiratory tract diseases
lcsh:Genetics
030104 developmental biology
chemistry
Cancer research
business
Zdroj: Non-coding RNA Research, Vol 3, Iss 4, Pp 161-173 (2018)
Non-coding RNA Research
ISSN: 2468-0540
Popis: Malignant mesothelioma diseases feature an increasing risk due to their severe forms and their association with asbestos exposure. Platinum(II) complexes such as cisplatin and carboplatin are clinically approved for the therapy of mesothelioma often in combination with antimetabolites such as pemetrexed or gemcitabine. It was observed that pathogenic properties of mesothelioma cells and the response of mesothelioma tumors towards platinum-based drugs are strongly influenced by non-coding RNAs, in particular, by small microRNAs (miRNAs) and long non-coding RNAs (lncRNAs). These non-coding RNAs controlled drug sensitivity and the development of tumor resistance towards platinum drugs. An overview of the interactions between platinum drugs and non-coding RNAs is given and the influence of non-coding RNAs on platinum drug efficacy in mesothelioma is discussed. Suitable non-coding RNA-modulating agents with potentially beneficial effects on cisplatin treatment of mesothelioma diseases are mentioned. The understanding of mesothelioma diseases concerning the interactions of non-coding RNAs and platinum drugs will optimize existing therapy schemes and pave the way to new treatment options in future. Keywords: MicroRNA, Long non-coding RNA, Mesothelioma, Cisplatin, Carboplatin, Anticancer drugs
Databáze: OpenAIRE