Accession Number:

AD1095698

Title:

Treatment-Induced Autophagy Associated with Tumor Dormancy and Relapse

Descriptive Note:

Technical Report,01 Jul 2014,30 Jun 2018

Corporate Author:

Virginia Commonwealth University Richmond United States

Personal Author(s):

Report Date:

2018-09-01

Pagination or Media Count:

41.0

Abstract:

Our finding can be broken down into three related components. I. Autophagy Dependent Tumor Dormancy. These studies indicate that use of pharmacologic agents such as chloroquine now being tested in multiple clinical trials could prolong chemotherapy induced cell arrest, which could contribute to a more durable disease remission. This type of transient blockade of autophagy does not affect breast tumor cell sensitivity to immunotherapy. In contrast, breast tumors that are intrinsically autophagy deficient may be more likely to contribute to recurrent disease furthermore, a sustained knockdown of autophagy also renders the tumor cells resistant to immunotherapy. Consequently, transient inhibition of autophagy would be the preferred approach to enhance breast cancer sensitivity to chemotherapy. II. Senescence Dependent Breast Cancer Dormancy and Sensitivity to Senolytic Agents. These studies demonstrate that cells in a state of senescence are capable of proliferative recovery, which may reflect a form of tumor dormancy. Furthermore, senolytic agents have the potential to attenuate or suppress proliferative recovery, suggesting their utilization to prevent breast cancer recurrence. Ongoing studies are designed to determine the impact of the senolytic agents combined with chemotherapeutics on the recognition and elimination of breast tumor cells by the immune system. III, Epigenetic regulation of tumor cell sensitivity to chemotherapy. These studies indicate that pharmacologic inhibition of NURF e.g. AU1 maybe effective in sensitizing breast tumor cells to chemotherapy, through both direct cell autonomous and indirect cell non-autonomous, immune mediated pathways.

Subject Categories:

  • Medicine and Medical Research
  • Anatomy and Physiology

Distribution Statement:

APPROVED FOR PUBLIC RELEASE