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Heterogeneity in hormone-dependent breast cancer and therapy : steroid hormones, HER2, melanoma antigens, and cannabinoid receptors
ID
Tavčar Kunstič, Tajda
(
Avtor
),
ID
Debeljak, Nataša
(
Avtor
),
ID
Fon Tacer, Klementina
(
Avtor
)
PDF - Predstavitvena datoteka,
prenos
(6,56 MB)
MD5: AA85EF7B56708A13C25EF109879934F3
URL - Izvorni URL, za dostop obiščite
https://www.sciencedirect.com/science/article/pii/S2667394022000600
Galerija slik
Izvleček
Breast cancer is the most frequently diagnosed cancer and the leading cause of death by cancer among women worldwide. The prognosis of the disease and patients’ response to different types of therapies varies in different subgroups of this heterogeneous disease. The subgroups are based on histological and molecular characteristics of the tumor, especially the expression of estrogen (ER) and progesterone receptor (PR), and human epidermal growth factor receptor 2 (HER2). Hormone-dependent breast cancer, determined predominantly by the presence of ER, is the most common type of breast cancer. Patients with hormone-dependent breast cancer have an available targeted therapy, however, tumor cells can develop resistance to the therapy, which is a major obstacle limiting the success of treatment and enabling relapse to metastatic disease. The complicated crosstalk of both tumor-intrinsic and exogenous factors may contribute to endocrine resistance, although the underlying molecular details are still enigmatic. For example, the expression of the melanoma antigen genes (MAGE) correlates with a worse clinical prognosis and therapy resistance in many types of cancers, including breast cancer. Recent studies suggested that cancers co-opt MAGEs’ physiological functions to promote therapy resistance and potentially metastasis development. The response to the therapy can be also affected by the concurrent use of alternative therapy, e.g., cannabinoid use is popular among breast cancer patients. Cannabinoids interact with endogenous estrogen function, however, how they interfere with breast cancer therapy is still poorly understood. In this review, we summarize the role of ER, PR, and HER2 in hormone-dependent breast cancer; provide current knowledge of MAGEs and cannabinoid receptors in breast cancer; ultimately discuss the potential interlacement of their signaling paths which may underlay diverse responses to therapies in breast cancer patients simultaneously using cannabinoids. These interactions are poorly understood but critical for the advancement of conventional and complementary treatment options for patients, particularly the ones with metastatic disease.
Jezik:
Angleški jezik
Ključne besede:
breast cancer
,
cannabinoids
,
hormone therapy
Vrsta gradiva:
Članek v reviji
Tipologija:
1.02 - Pregledni znanstveni članek
Organizacija:
MF - Medicinska fakulteta
Datum objave:
01.01.2023
Leto izida:
2023
Št. strani:
Str. 1-12
Številčenje:
Vol. 7
PID:
20.500.12556/RUL-165015
UDK:
616-006
ISSN pri članku:
2667-3940
DOI:
10.1016/j.adcanc.2022.100086
COBISS.SI-ID:
136998915
Datum objave v RUL:
21.11.2024
Število ogledov:
20
Število prenosov:
1
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Objavi na:
Gradivo je del revije
Naslov:
Advances in cancer biology. Metastasis
Založnik:
Elsevier
ISSN:
2667-3940
COBISS.SI-ID:
87457795
Licence
Licenca:
CC BY-NC-ND 4.0, Creative Commons Priznanje avtorstva-Nekomercialno-Brez predelav 4.0 Mednarodna
Povezava:
http://creativecommons.org/licenses/by-nc-nd/4.0/deed.sl
Opis:
Najbolj omejujoča licenca Creative Commons. Uporabniki lahko prenesejo in delijo delo v nekomercialne namene in ga ne smejo uporabiti za nobene druge namene.
Sekundarni jezik
Jezik:
Slovenski jezik
Ključne besede:
rak dojke
,
kanabinoidi
,
hormonska terapija
Projekti
Financer:
Drugi - Drug financer ali več financerjev
Program financ.:
Texas Tech University School of Veterinary Medicine start up (to K.F.T)
Financer:
Drugi - Drug financer ali več financerjev
Program financ.:
Cancer Prevention and REsearch Instiute of Texas Scholar Award
Številka projekta:
RR200059 (to K.F.T.)
Financer:
Drugi - Drug financer ali več financerjev
Program financ.:
Foundation for Prader-Willi Syndrome Research Grant
Številka projekta:
22-0321 (to K.F.T.)
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