% IMPORTANT: The following is UTF-8 encoded. This means that in the presence
% of non-ASCII characters, it will not work with BibTeX 0.99 or older.
% Instead, you should use an up-to-date BibTeX implementation like “bibtex8” or
% “biber”.
@ARTICLE{Xia:284655,
author = {P. Xia and A. Dubrovska$^*$},
title = {{CD}98 heavy chain as a prognostic biomarker and target for
cancer treatment.},
journal = {Frontiers in oncology},
volume = {13},
issn = {2234-943X},
address = {Lausanne},
publisher = {Frontiers Media},
reportid = {DKFZ-2023-02056},
pages = {1251100},
year = {2023},
abstract = {The SLC3A2 gene encodes for a cell-surface transmembrane
protein CD98hc (4F2). CD98hc serves as a chaperone for LAT1
(SLC7A5), LAT2 (SLC7A8), y+LAT1 (SLC7A7), y+LAT2 (SLC7A6),
xCT (SLC7A11) and Asc1 (SLC7A10) providing their recruitment
to the plasma membrane. Together with the light subunits, it
constitutes heterodimeric transmembrane amino acid
transporters. CD98hc interacts with other surface molecules,
such as extracellular matrix metalloproteinase inducer CD147
(EMMPRIN) and adhesion receptors integrins, and regulates
glucose uptake. In this way, CD98hc connects the signaling
pathways sustaining cell proliferation and migration,
biosynthesis and antioxidant defense, energy production, and
stem cell properties. This multifaceted role makes CD98hc
one of the critical regulators of tumor growth, therapy
resistance, and metastases. Indeed, the high expression
levels of CD98hc were confirmed in various tumor tissues,
including head and neck squamous cell carcinoma,
glioblastoma, colon adenocarcinoma, pancreatic ductal
adenocarcinoma, and others. A high expression of CD98hc has
been linked to clinical prognosis and response to chemo- and
radiotherapy in several types of cancer. In this
mini-review, we discuss the physiological functions of
CD98hc, its role in regulating tumor stemness, metastases,
and therapy resistance, and the clinical significance of
CD98hc as a tumor marker and therapeutic target.},
subtyp = {Review Article},
keywords = {CD98hc (Other) / CSC: cancer stem cell (Other) / LAT1
(Other) / ferroptosis (Other) / therapy resistance (Other) /
tumor progression (Other) / xCT (Other)},
cin = {DD01},
ddc = {610},
cid = {I:(DE-He78)DD01-20160331},
pnm = {899 - ohne Topic (POF4-899)},
pid = {G:(DE-HGF)POF4-899},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:37823053},
pmc = {pmc:PMC10562705},
doi = {10.3389/fonc.2023.1251100},
url = {https://inrepo02.dkfz.de/record/284655},
}