Stromal cells downregulate miR-23a-5p to activate protective autophagy in acute myeloid leukemia.
|Title||Stromal cells downregulate miR-23a-5p to activate protective autophagy in acute myeloid leukemia.|
|Publication Type||Journal Article|
|Year of Publication||2019|
|Authors||Ganesan S, Palani HKumar, Lakshmanan V, Balasundaram N, Alex AAbu, David S, Venkatraman A, Korula A, George B, Balasubramanian P, Palakodeti D, Vyas N, Mathews V|
|Journal||Cell Death Dis|
|Date Published||2019 Sep 30|
Complex molecular cross talk between stromal cells and the leukemic cells in bone marrow is known to contribute significantly towards drug-resistance. Here, we have identified the molecular events that lead to stromal cells mediated therapy-resistance in acute myeloid leukemia (AML). Our work demonstrates that stromal cells downregulate miR-23a-5p levels in leukemic cells to protect them from the chemotherapy induced apoptosis. Downregulation of miR-23a-5p in leukemic cells leads to upregulation of protective autophagy by targeting TLR2 expression. Further, autophagy inhibitors when used as adjuvants along with conventional drugs can improve drug sensitivity in vitro as well in vivo in a mouse model of leukemia. Our work also demonstrates that this mechanism of bone marrow stromal cell mediated regulation of miR-23a-5p levels and subsequent molecular events are relevant predominantly in myeloid leukemia. Our results illustrate the critical and dynamic role of the bone marrow microenvironment in modulating miRNA expression in leukemic cells which could contribute significantly to drug resistance and subsequent relapse, possibly through persistence of minimal residual disease in this environment.
|Alternate Journal||Cell Death Dis|
|PubMed Central ID||PMC6769009|
|Grant List||IA/S/11/2500267 / / DBT India Alliance (Wellcome Trust/DBT India Alliance) / |
BT/COE/34/SP13432/2015 / / Department of Biotechnology, Ministry of Science and Technology (DBT) /
ECR/2016/ 000251 / / Department of Science and Technology, Ministry of Science and Technology (DST) /