2022
DOI: 10.1016/j.freeradbiomed.2022.07.019
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Diallyl trisulfide sensitizes radiation therapy on glioblastoma through directly targeting thioredoxin 1

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Cited by 6 publications
(4 citation statements)
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“…Furthermore, DAST has been shown to enhance irradiation (IR)-induced ROS accumulation, apoptosis, and DNA damage, and inhibit tumor growth of GBM cells as well. These observations suggest the utility of DATS in sensitizing radiotherapy to GBM patients [142].…”
Section: Diallyl Trisulfide (Dast)mentioning
confidence: 76%
“…Furthermore, DAST has been shown to enhance irradiation (IR)-induced ROS accumulation, apoptosis, and DNA damage, and inhibit tumor growth of GBM cells as well. These observations suggest the utility of DATS in sensitizing radiotherapy to GBM patients [142].…”
Section: Diallyl Trisulfide (Dast)mentioning
confidence: 76%
“…Also, in our previous work performed on colorectal cancer cells, IC50 of PTX was in the nanomolar range, and IC50 of GYY4137 was in the micromolar range, showing a low toxicity of GYY4137 after 24h treatment [ 9 ]. Since GYY4137 and other sulfide donors were already shown to potentiate apoptosis in cancer cells [ 31 , 32 , 33 ], we first evaluated the effect of GYY4137 on the level of apoptosis. Co-treatment of GYY4137 with PTX potentiated apoptosis in MDA-MB-231 cells, but not in JIMT1 cells, thus pointing to the diverse effect of exogenous H 2 S on different types of breast cancer cells.…”
Section: Discussionmentioning
confidence: 99%
“…This strategy aims to enhance the drugs' specificity in application. For instance, Trx1 inhibitors may exhibit heightened efficacy against cancer that rely on Trx1 for survival and proliferation, while Trx2 inhibitors could be more effective against certain ND resulting from mitochondrial dysfunction and oxidative stress [ 282 , 377 ]. The final objective is to optimize the utilization of predictive factors prior to treatment, thereby facilitating a more comprehensive evaluation of the expression and activity disparities among Trx system constituents in both normal and pathological cells.…”
Section: Therapeutic Potential Of Trx Proteins In Aging Diseasesmentioning
confidence: 99%
“… Diallyl trisulfide (DATS)→Trx1→Glioblastoma Sorafenib→Trx1→Hepatocellular carcinoma (NCT00618384, NCT01029418, NCT01029418, NCT00892658, NCT00846131, NCT00846131, etc.) [ 487 ] [ 377 ] [ 488 ] TrxR TrxR-interfering drug delivery system (based on RGD-PEG-PUSeSe-PEG-RGD self-assembling micelles)→TrxR→Cancer Se-methylselenocysteine (SMC)→TrxR→AD (NCT01497431, etc.) Butaselen (BS)→TrxR1→Hepatocellular carcinoma BBSKE (Ethaselen)→TrxR1→Cancer ACZ2→TrxR1→Gastric cancer Ethaselen→TrxR1→Lung cancer [ 360 ] [ 489 ] [ 490 ] [ 491 ] [ 492 ] [ 493 ] Michael receptor TrxR [ 6 ]-dehydroshogaol→TrxR→Cancer DVD-445 and its extended analogues→TrxR→Cancer [ 494 ] [ 495 ] Quinazoline derivatives TXNIP Quinazoline derivatives (D-2 & C-1)→TXNIP→Diabetes [ 496 ] Imidazole derivatives Trx1 PX-12 (1-methylpropyl 2-imidazolyl disulfide)→Trx1→Cancer [ 497 ] Benzopyrane derivatives Trx & TrxR SIMR1281→Trx & TrxR→Cancer [ 498 ] Other compounds and therapeutic methods Trx Ac-Cys-Pro-Cys-amide (thioredoxin-mimetic peptide)→Atherosclerosis …”
Section: Therapeutic Potential Of Trx Proteins In Aging Diseasesmentioning
confidence: 99%