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10.1208/s12248-014-9705-5

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suck abstract from ncbi


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pmid25466495
      AAPS+J 2015 ; 17 (2 ): 313-22
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  • Vitamin E transporters in cancer therapy #MMPMID25466495
  • Alqahtani S ; Kaddoumi A
  • AAPS J 2015[Mar]; 17 (2 ): 313-22 PMID25466495 show ga
  • Besides their potent antioxidant activity, vitamin E isoforms demonstrated multiple therapeutic activities among which is their activity against different cancer types, including breast, prostate, and colon cancers. However, the activity of vitamin E isoforms is limited by their low bioavailability following oral administration. In addition to the low solubility, vitamin E isoforms have been established as substrates for several intestinal and hepatic transport proteins. In this review, we present reported anticancer activity of vitamin E family members and the possible utilization of vitamin E and derivatives as chemosensitizers to reverse multidrug resistance when given as part of a delivery system and/or in combination with anticancer therapeutic drugs. Then, the review discusses disposition of vitamin E members and transport proteins that play a role in determining their systemic bioavailability followed by recent advances in vitamin E formulations and delivery strategies.
  • |Administration, Oral [MESH]
  • |Animals [MESH]
  • |Antineoplastic Agents/*administration & dosage/chemistry/pharmacokinetics [MESH]
  • |Antioxidants/administration & dosage/chemistry/pharmacokinetics [MESH]
  • |Biological Availability [MESH]
  • |Biological Transport [MESH]
  • |Drug Resistance, Neoplasm [MESH]
  • |Humans [MESH]
  • |Membrane Transport Proteins/metabolism [MESH]
  • |Neoplasms/*drug therapy/pathology [MESH]
  • |Solubility [MESH]


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