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RETRACTED: Synthetic Makaluvamine Analogs Decrease c-Kit Expression and Are Cytotoxic to Neuroendocrine Tumor Cells
Zviadi Aburjania1, Jason D Whitt1, Samuel Jang1
1Department of Surgery, University of Alabama at Birmingham, 1824 6th Avenue S., Birmingham, AL 35233, USA.
Abstract:
In an effort to discover viable systemic chemotherapeutic agents for neuroendocrine tumors (NETs), we screened a small library of 18 drug-like compounds obtained from the Velu lab against pulmonary (H727) and thyroid (MZ-CRC-1 and TT) neuroendocrine tumor-derived cell lines. Two potent lead compounds (DHN-II-84 and DHN-III-14) identified from this screening were found to be analogs of the natural product makaluvamine. We further characterized the antitumor activities of these two compounds using pulmonary (H727), thyroid (MZ-CRC-1) and pancreatic (BON) neuroendocrine tumor cell lines. Flow cytometry showed a dose-dependent increase in apoptosis in all cell lines. Induction of apoptosis with these compounds was also supported by the decrease in myeloid cell leukemia-1 (MCL-1) and X-chromosome linked inhibitor of apoptosis (XIAP) detected by Western blot. Compound treatment decreased NET markers chromogranin A (CgA) and achaete-scute homolog 1 (ASCL1) in a dose-dependent manner. Moreover, the gene expression analysis showed that the compound treatment reduced c-Kit proto-oncogene expression in the NET cell lines. Induction of apoptosis could also have been caused by the inhibition of c-Kit expression, in addition to the known mechanisms such as damage of DNA by topoisomerase II inhibition for this class of compounds. In summary, makaluvamine analogs DHN-II-84 and DHN-III-14 induced apoptosis, decreased neuroendocrine tumor markers, and showed promising antitumor activity in pulmonary, thyroid, and pancreatic NET cell lines, and hold potential to be developed as an effective treatment to combat neuroendocrine tumors.
Insights
Two makaluvamine analogs, DHN-II-84 and DHN-III-14, show potent antitumor activity against neuroendocrine tumors (NETs). These compounds induce apoptosis and decrease key NET markers, offering potential for new NET chemotherapy.
Area of Science:
- Oncology
- Pharmacology
- Molecular Biology
Background:
- Neuroendocrine tumors (NETs) require novel systemic chemotherapeutic agents.
- Existing treatments have limitations, necessitating the discovery of new therapeutic strategies.
Purpose of the Study:
- To screen a library of drug-like compounds for activity against NET cell lines.
- To characterize the antitumor mechanisms of promising lead compounds, DHN-II-84 and DHN-III-14.
Main Methods:
- Screening of 18 compounds against pulmonary and thyroid NET cell lines.
- Flow cytometry and Western blot analysis to assess apoptosis and protein levels (MCL-1, XIAP).
- Gene expression analysis to evaluate c-Kit proto-oncogene and NET marker (CgA, ASCL1) expression.
Main Results:
- Two makaluvamine analogs, DHN-II-84 and DHN-III-14, demonstrated potent antitumor activity.
- Compounds induced dose-dependent apoptosis in pulmonary, thyroid, and pancreatic NET cell lines.
- Treatment decreased NET markers (CgA, ASCL1) and c-Kit expression, with apoptosis linked to c-Kit inhibition.
Conclusions:
- Makaluvamine analogs DHN-II-84 and DHN-III-14 exhibit significant antitumor potential for NETs.
- These compounds effectively induce apoptosis and reduce critical NET markers.
- Further development of these analogs could lead to novel treatments for neuroendocrine tumors.
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