GLUT1 participates in tamoxifen resistance in breast cancer cells through autophagy regulation
Tamoxifen is an estrogen modulator widely used in the treatment of patients with ESR/ER-positive breast cancer; however, resistance limits its clinical application. Autophagy alterations have recently been suggested as a new mechanism for tamoxifen resistance. Glucose transporter 1 (GLUT1) has been reported to be associated with the development and metastasis of breast cancer, but the relationship among GLUT1, autophagy, and endocrine resistance remains unclear. Our present study found that GLUT1 expression and autophagy flux were upregulated in the tamoxifen-resistant breast cancer cell line MCF-7/TAMR-1 and that knockdown of GLUT1 promoted sensitization to tamoxifen. Moreover, knockdown of GLUT1 significantly decreased the enhancement of autophagy flux in tamoxifen-resistant cell lines. Furthermore, inhibiting autophagy in tamoxifen-resistant cells resulted in sensitization to tamoxifen. We conclude that GLUT1 contributes to tamoxifen resistance in breast cancer and that tamoxifen-resistant cells become resensitized to tamoxifen after GLUT1 silencing. These findings suggest GLUT1 as a new factor clinically associated with resistance to tamoxifen.
Medienart: |
E-Artikel |
---|
Erscheinungsjahr: |
2021 |
---|---|
Erschienen: |
2021 |
Enthalten in: |
Zur Gesamtaufnahme - volume:394 |
---|---|
Enthalten in: |
Naunyn-Schmiedeberg's archives of pharmacology - 394(2021), 1 vom: 05. Jan., Seite 205-216 |
Sprache: |
Englisch |
---|
Beteiligte Personen: |
Sun, Mengqi [VerfasserIn] |
---|
Links: |
---|
Anmerkungen: |
Date Completed 19.10.2021 Date Revised 19.10.2021 published: Print-Electronic Citation Status MEDLINE |
---|
doi: |
10.1007/s00210-020-01893-3 |
---|
funding: |
|
---|---|
Förderinstitution / Projekttitel: |
|
PPN (Katalog-ID): |
NLM310797624 |
---|
LEADER | 01000naa a22002652 4500 | ||
---|---|---|---|
001 | NLM310797624 | ||
003 | DE-627 | ||
005 | 20231225140851.0 | ||
007 | cr uuu---uuuuu | ||
008 | 231225s2021 xx |||||o 00| ||eng c | ||
024 | 7 | |a 10.1007/s00210-020-01893-3 |2 doi | |
028 | 5 | 2 | |a pubmed24n1035.xml |
035 | |a (DE-627)NLM310797624 | ||
035 | |a (NLM)32500187 | ||
040 | |a DE-627 |b ger |c DE-627 |e rakwb | ||
041 | |a eng | ||
100 | 1 | |a Sun, Mengqi |e verfasserin |4 aut | |
245 | 1 | 0 | |a GLUT1 participates in tamoxifen resistance in breast cancer cells through autophagy regulation |
264 | 1 | |c 2021 | |
336 | |a Text |b txt |2 rdacontent | ||
337 | |a ƒaComputermedien |b c |2 rdamedia | ||
338 | |a ƒa Online-Ressource |b cr |2 rdacarrier | ||
500 | |a Date Completed 19.10.2021 | ||
500 | |a Date Revised 19.10.2021 | ||
500 | |a published: Print-Electronic | ||
500 | |a Citation Status MEDLINE | ||
520 | |a Tamoxifen is an estrogen modulator widely used in the treatment of patients with ESR/ER-positive breast cancer; however, resistance limits its clinical application. Autophagy alterations have recently been suggested as a new mechanism for tamoxifen resistance. Glucose transporter 1 (GLUT1) has been reported to be associated with the development and metastasis of breast cancer, but the relationship among GLUT1, autophagy, and endocrine resistance remains unclear. Our present study found that GLUT1 expression and autophagy flux were upregulated in the tamoxifen-resistant breast cancer cell line MCF-7/TAMR-1 and that knockdown of GLUT1 promoted sensitization to tamoxifen. Moreover, knockdown of GLUT1 significantly decreased the enhancement of autophagy flux in tamoxifen-resistant cell lines. Furthermore, inhibiting autophagy in tamoxifen-resistant cells resulted in sensitization to tamoxifen. We conclude that GLUT1 contributes to tamoxifen resistance in breast cancer and that tamoxifen-resistant cells become resensitized to tamoxifen after GLUT1 silencing. These findings suggest GLUT1 as a new factor clinically associated with resistance to tamoxifen | ||
650 | 4 | |a Journal Article | |
650 | 4 | |a Autophagy | |
650 | 4 | |a Breast cancer | |
650 | 4 | |a GLUT1 | |
650 | 4 | |a Tamoxifen resistance | |
650 | 7 | |a Antineoplastic Agents, Hormonal |2 NLM | |
650 | 7 | |a Estrogen Antagonists |2 NLM | |
650 | 7 | |a Glucose Transporter Type 1 |2 NLM | |
650 | 7 | |a RNA, Small Interfering |2 NLM | |
650 | 7 | |a SLC2A1 protein, human |2 NLM | |
650 | 7 | |a Tamoxifen |2 NLM | |
650 | 7 | |a 094ZI81Y45 |2 NLM | |
700 | 1 | |a Zhao, Shu |e verfasserin |4 aut | |
700 | 1 | |a Duan, Yuchen |e verfasserin |4 aut | |
700 | 1 | |a Ma, Yumeng |e verfasserin |4 aut | |
700 | 1 | |a Wang, Yicheng |e verfasserin |4 aut | |
700 | 1 | |a Ji, Hongfei |e verfasserin |4 aut | |
700 | 1 | |a Zhang, Qingyuan |e verfasserin |4 aut | |
773 | 0 | 8 | |i Enthalten in |t Naunyn-Schmiedeberg's archives of pharmacology |d 1972 |g 394(2021), 1 vom: 05. Jan., Seite 205-216 |w (DE-627)NLM000008354 |x 1432-1912 |7 nnns |
773 | 1 | 8 | |g volume:394 |g year:2021 |g number:1 |g day:05 |g month:01 |g pages:205-216 |
856 | 4 | 0 | |u http://dx.doi.org/10.1007/s00210-020-01893-3 |3 Volltext |
912 | |a GBV_USEFLAG_A | ||
912 | |a GBV_NLM | ||
951 | |a AR | ||
952 | |d 394 |j 2021 |e 1 |b 05 |c 01 |h 205-216 |