A critical evaluation of the mechanisms of action proposed for the antitumor effects of the anthracycline antibiotics adriamycin and daunorubicin
DA Gewirtz - Biochemical pharmacology, 1999 - Elsevier
The mechanisms responsible for the antiproliferative and cytotoxic effects of the
anthracycline antibiotics doxorubicin (Adriamycin®) and daunorubicin (daunomycin) have …
anthracycline antibiotics doxorubicin (Adriamycin®) and daunorubicin (daunomycin) have …
The challenge of drug resistance in cancer treatment: a current overview
It is generally accepted that recent advances in anticancer agents have contributed
significantly to the improvement of both the disease-free survival and quality of life in cancer …
significantly to the improvement of both the disease-free survival and quality of life in cancer …
Multidrug resistance (MDR) in cancer: mechanisms, reversal using modulators of MDR and the role of MDR modulators in influencing the pharmacokinetics of …
R Krishna, LD Mayer - European journal of pharmaceutical sciences, 2000 - Elsevier
In recent years, there has been an increased understanding of P-glycoprotein (P-GP)-
mediated pharmacokinetic interactions. In addition, its role in modifying the bioavailability of …
mediated pharmacokinetic interactions. In addition, its role in modifying the bioavailability of …
Doxorubicin (adriamycin): a critical review of free radical-dependent mechanisms of cytotoxicity
HG Keizer, HM Pinedo, GJ Schuurhuis… - Pharmacology & …, 1990 - Elsevier
The antineoplastic drug doxorubicin is capable of generating a variety of free radical species
in subcellular systems and this capacity has been considered critical for its antitumor action …
in subcellular systems and this capacity has been considered critical for its antitumor action …
How do chemotherapeutic agents damage the ovary?
BACKGROUND Chemotherapy treatment in premenopausal women is associated with an
increased risk of premature ovarian failure (POF) but the exact mechanism through which …
increased risk of premature ovarian failure (POF) but the exact mechanism through which …
Increasing role of the cancer chemotherapeutic doxorubicin in cellular metabolism
AM Meredith, CR Dass - Journal of Pharmacy and …, 2016 - academic.oup.com
Objectives The use of doxorubicin, a drug utilised for many years to treat a wide variety of
cancers, has long been limited due to the significant toxicity that can occur not only during …
cancers, has long been limited due to the significant toxicity that can occur not only during …
Coadministration of paclitaxel and curcumin in nanoemulsion formulations to overcome multidrug resistance in tumor cells
Development of multidrug resistance (MDR) against a variety of conventional and novel
chemotherapeutic agents is a significant challenge in effective cancer therapy. Over the last …
chemotherapeutic agents is a significant challenge in effective cancer therapy. Over the last …
Paclitaxel and quercetin co-loaded functional mesoporous silica nanoparticles overcoming multidrug resistance in breast cancer
M Liu, M Fu, X Yang, G Jia, X Shi, J Ji, X Liu… - Colloids and Surfaces B …, 2020 - Elsevier
Multidrug resistance (MDR) in tumor has long been considered a major factor in the failure
of tumor chemotherapy. P-glycoprotein (P-gp)-mediated drug efflux plays a significant role in …
of tumor chemotherapy. P-glycoprotein (P-gp)-mediated drug efflux plays a significant role in …
[BOOK][B] Cancer chemotherapy and biotherapy: principles and practice
K Tew, OM Colvin, BA Chabner - 1996 - doctorlib.info
The alkylating agents are antitumor drugs that act through the covalent binding of alkyl
groups to cellular molecules. This binding is mediated by reactive intermediates formed from …
groups to cellular molecules. This binding is mediated by reactive intermediates formed from …
Quercetin potentiates the effect of adriamycin in a multidrug-resistant MCF-7 human breast-cancer cell line: P-glycoprotein as a possible target
G Scambia, FO Ranelletti, PB Panici… - Cancer chemotherapy …, 1994 - Springer
This study demonstrates that the flavonoid quercetin (Q), a plant-derived compound with low
toxicity in vivo, greatly potentiates the growth-inhibitory activity of Adriamycin (ADR) on MCF …
toxicity in vivo, greatly potentiates the growth-inhibitory activity of Adriamycin (ADR) on MCF …