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Targeting Her2-Positive Breast Cance...
~
Rainey, Magdalena A.
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Targeting Her2-Positive Breast Cancer Metabolism Through Dietary and Pharmacological Interventions to Improve Therapeutic Efficacy.
紀錄類型:
書目-電子資源 : Monograph/item
正題名/作者:
Targeting Her2-Positive Breast Cancer Metabolism Through Dietary and Pharmacological Interventions to Improve Therapeutic Efficacy./
作者:
Rainey, Magdalena A.
出版者:
Ann Arbor : ProQuest Dissertations & Theses, : 2019,
面頁冊數:
74 p.
附註:
Source: Masters Abstracts International, Volume: 80-12.
Contained By:
Masters Abstracts International80-12.
標題:
Pharmacology. -
電子資源:
http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=13858921
ISBN:
9781392203224
Targeting Her2-Positive Breast Cancer Metabolism Through Dietary and Pharmacological Interventions to Improve Therapeutic Efficacy.
Rainey, Magdalena A.
Targeting Her2-Positive Breast Cancer Metabolism Through Dietary and Pharmacological Interventions to Improve Therapeutic Efficacy.
- Ann Arbor : ProQuest Dissertations & Theses, 2019 - 74 p.
Source: Masters Abstracts International, Volume: 80-12.
Thesis (M.S.)--The University of North Carolina at Chapel Hill, 2019.
This item must not be sold to any third party vendors.
HER2-positive breast cancers (HER2+ BC) are an aggressive subset characterized by therapeutic resistance in ∼40-60% of patients. We hypothesized that modulating energy-responsive pathways through either dietary restriction or pharmacological metabolic reprogramming interventions (MRI) would increase the efficacy of HER2-directed therapies trastuzumab and lapatinib. Dietary restriction was modeled in vitro and the efficacy of lapatinib was increased under serum-restricted conditions. This effect was recapitulated with MRIs and we determined that inhibition of IGF1R/insulin receptor and mTORC1 increased the antiproliferative effects of lapatinib. Ongoing work is investigating the impact of intermittent fasting regimens on therapeutic efficacy in vivo by restricting the dietary intake of mice with HER2+ BC for 48 hours coinciding with the administration of trastuzumab or lapatinib. We conclude that inhibition of metabolic pathways implicated in HER2+ BC drug resistance through intermittent fasting regimens and pharmacological MRIs has the potential to increase the efficacy of HER2-directed therapies.
ISBN: 9781392203224Subjects--Topical Terms:
634543
Pharmacology.
Targeting Her2-Positive Breast Cancer Metabolism Through Dietary and Pharmacological Interventions to Improve Therapeutic Efficacy.
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HER2-positive breast cancers (HER2+ BC) are an aggressive subset characterized by therapeutic resistance in ∼40-60% of patients. We hypothesized that modulating energy-responsive pathways through either dietary restriction or pharmacological metabolic reprogramming interventions (MRI) would increase the efficacy of HER2-directed therapies trastuzumab and lapatinib. Dietary restriction was modeled in vitro and the efficacy of lapatinib was increased under serum-restricted conditions. This effect was recapitulated with MRIs and we determined that inhibition of IGF1R/insulin receptor and mTORC1 increased the antiproliferative effects of lapatinib. Ongoing work is investigating the impact of intermittent fasting regimens on therapeutic efficacy in vivo by restricting the dietary intake of mice with HER2+ BC for 48 hours coinciding with the administration of trastuzumab or lapatinib. We conclude that inhibition of metabolic pathways implicated in HER2+ BC drug resistance through intermittent fasting regimens and pharmacological MRIs has the potential to increase the efficacy of HER2-directed therapies.
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