Abstract 678P
Background
Cancer stem cells (CSCs) are the major cause of therapy failure. CSCs are responsible for cancer relapse, metastasis, chemo-resistance, and radiation resistance. Therefore, targeting CSCs is imperative for better therapy outcomes. To date, there is no therapy precisely targeting CSCs. To fill these lacunae we have developed ExoDS a bioengineered exosome-based platform to precisely deliver chemotherapy drugs directly to CSCs effectively eliminating them.
Methods
ExoDS is an exosome-based platform that has been isolated and purified from immune cells that have been treated with a patented bioformulation and the specific drug to be incorporated within exosomes. To test the efficacy of ExoDS in targeting CSCs, we first generated and isolated CSCs from breast cancer cell lines, MCF7, MDA-MB-231, and MDA-MB-468. We next isolated CSCs from chemo-naïve breast tumor tissue samples to test the efficacy of ExoDS in targeting breast CSCs. We extensively used flow cytometric dependent analysis of AnnexinV to determine apoptosis in CSCs.
Results
Our results have shown that ExoDS can specifically identify and target CSCs with a 12-fold higher efficiency as compared to free drugs. At a cellular level, we established that ExoDS gets internalized inside CSCs within 6hrs of treatment. ExoDS was also found to target CTCs isolated from patient blood (n=5). Further analysis revealed that ExoDS spared healthy PBMCs isolated from healthy donors (n=9) as well as breast cancer patients (n=7). Our data confirmed that ExoDS can reduce chemotoxicity by more than 30%. Broadly, our results highlight the benefits of using ExoDS as compared to free chemotherapy drugs. ExoDS is a potential chemotherapy alternative.
Conclusions
Collectively, ExoDS efficiently targeted CSC in-vitro and also ex-vivo. Its specificity towards CSCs was established by the inability of ExoDS to target PBMCs derived from healthy individuals as well as patients. ExoDS can potentially target CSCs in a clinical setting making it a first-of-its-kind therapy vehicle. Targeting CSCs will revolutionize cancer treatments and will lead to better therapy outcomes. Currently, we are testing ExoDS in murine models to test it's in vivo efficacy and efficiency.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
Exsure.
Funding
Biotechnology Industry Research Assistance Council (BIRAC), Government of India.
Disclosure
A. Dutta, S. Paul, S. Bhagat: Financial Interests, Institutional, Full or part-time Employment: Exsure.
Resources from the same session
97P - Neoadjuvant durvalumab plus gemcitabine and cisplatin (D+GemCis) versus gemcis alone for localized biliary tract cancer (BTC): Results of a randomized, multicenter, open-label, phase II trial (DEBATE)
Presenter: Changhoon Yoo
Session: Poster session 17
101P - Quality of life (QoL) outcomes in patients (pts) with zanidatamab (zani)-treated HER2-positive (HER2+) biliary tract cancer (BTC) in the phase IIb HERIZON-BTC-01 study
Presenter: Harpreet Wasan
Session: Poster session 17
102P - Potentially prognostic factors of overall survival in advanced biliary tract cancer in the randomised phase III TOPAZ-1 study
Presenter: Aiwu Ruth He
Session: Poster session 17
103P - Individual patient data (IPD) meta-analysis of randomised trials to compare efficacy of second-line fluoropyrimidine-based chemotherapy in advanced biliary tract cancer (BTC)
Presenter: Jaewon Hyung
Session: Poster session 17
104P - Final analysis of the prospective, randomized phase II STAMP trial: Adjuvant gemcitabine plus cisplatin (GemCis) versus capecitabine (CAP) in node-positive extrahepatic cholangiocarcinoma (CCA)
Presenter: Hyehyun Jeong
Session: Poster session 17
105P - A phase II study of SHR-1316 plus IBI310 in patients with advanced intrahepatic cholangiocarcinoma after failure of first-line therapy
Presenter: Jia Fan
Session: Poster session 17