Detailed Information on Publication Record
2021
Cell death in head and neck cancer pathogenesis and treatment
RAUDENSKÁ, Martina, Jan BALVAN and Michal MASAŘÍKBasic information
Original name
Cell death in head and neck cancer pathogenesis and treatment
Authors
RAUDENSKÁ, Martina (203 Czech Republic, belonging to the institution), Jan BALVAN (203 Czech Republic, belonging to the institution) and Michal MASAŘÍK (203 Czech Republic, guarantor, belonging to the institution)
Edition
CELL DEATH & DISEASE, LONDON, NATURE PUBLISHING GROUP, 2021, 2041-4889
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
10601 Cell biology
Country of publisher
United Kingdom of Great Britain and Northern Ireland
Confidentiality degree
není předmětem státního či obchodního tajemství
References:
Impact factor
Impact factor: 9.685
RIV identification code
RIV/00216224:14110/21:00119012
Organization unit
Faculty of Medicine
UT WoS
000621062800002
Keywords in English
Cell death; head and neck cancer; pathogenesis; treatment
Tags
International impact, Reviewed
Změněno: 15/6/2021 09:13, Mgr. Tereza Miškechová
Abstract
V originále
Many cancer therapies aim to trigger apoptosis in cancer cells. Nevertheless, the presence of oncogenic alterations in these cells and distorted composition of tumour microenvironment largely limit the clinical efficacy of this type of therapy. Luckily, scientific consensus describes about 10 different cell death subroutines with different regulatory pathways and cancer cells are probably not able to avoid all of cell death types at once. Therefore, a focused and individualised therapy is needed to address the specific advantages and disadvantages of individual tumours. Although much is known about apoptosis, therapeutic opportunities of other cell death pathways are often neglected. Molecular heterogeneity of head and neck squamous cell carcinomas (HNSCC) causing unpredictability of the clinical response represents a grave challenge for oncologists and seems to be a critical component of treatment response. The large proportion of this clinical heterogeneity probably lies in alterations of cell death pathways. How exactly cells die is very important because the predominant type of cell death can have multiple impacts on the therapeutic response as cell death itself acts as a second messenger. In this review, we discuss the different types of programmed cell death (PCD), their connection with HNSCC pathogenesis and possible therapeutic windows that result from specific sensitivity to some form of PCD in some clinically relevant subgroups of HNSCC.
Links
GA18-03978S, research and development project |
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MUNI/A/1246/2020, interní kód MU |
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MUNI/A/1698/2020, interní kód MU |
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NU20J-08-00018, research and development project |
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