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Published on: September 3, 2021
AVJ16 inhibits lung carcinoma by targeting IGF2BP1
Nadav Wallis1,2, Tehila Gershon3, Sojod Shaaby3
1Department of Developmental Biology and Cancer Research, Institute for Medical Research - Israel-Canada, Hebrew University Hadassah Medical School, Jerusalem, Israel. nadavwallis@gmail.com.
Abstract:
IGF2BP1 is an oncofoetal RNA binding protein (RBP) expressed in many tumors. Interest has focused of late on the role of RBPs in cancer, although their mechanism of action is not always well understood. Using a newly described small molecule inhibitor of IGF2BP1, termed AVJ16, we have analyzed the effects of this inhibition on RNA binding, RNA expression, and protein expression. AVJ16 treatment downregulates RNAs encoding members of several pro-oncogenic signaling pathways, including Hedgehog, Wnt, and PI3K-Akt, and there is a strong correlation between IGF2BP1 RNA binding, RNA expression, and protein expression. At the cellular level, colony formation, invasion, and spheroid growth are all strongly reduced by exposure to AVJ16, while apoptosis and cell death are enhanced. All of these effects are limited to cells expressing IGF2BP1. In syngeneic LUAD xenografts in mice, IP injection of AVJ16 prevents tumor growth, and incubation with AVJ16 induces cell death in human organoids derived from IGF2BP1-expressing LUADs but not from healthy lung tissue. These results demonstrate that AVJ16 is a promising candidate for targeted therapy directed against tumors expressing IGF2BP1.
Insights
A new inhibitor, AVJ16, targets the oncofoetal protein IGF2BP1 (Insulin-like Growth Factor 2 Binding Protein 1). This drug reduces tumor growth and promotes cell death in cancers expressing IGF2BP1, showing promise for targeted cancer therapy.
Area of Science:
- Oncology
- Molecular Biology
- Drug Discovery
Background:
- Insulin-like Growth Factor 2 Binding Protein 1 (IGF2BP1) is an oncofoetal RNA binding protein (RBP) implicated in various cancers.
- The precise mechanisms of RBPs in cancer progression are not fully elucidated.
- Targeting specific RBPs offers a potential strategy for novel cancer therapies.
Purpose of the Study:
- To investigate the effects of a novel small molecule inhibitor, AVJ16, on IGF2BP1 activity and its downstream consequences in cancer cells.
- To evaluate the therapeutic potential of AVJ16 in preclinical cancer models.
Main Methods:
- Treatment of cancer cells and xenografts with AVJ16.
- Analysis of RNA binding, RNA expression, and protein expression.
- Assessment of cellular phenotypes including colony formation, invasion, spheroid growth, apoptosis, and cell death.
- Evaluation in syngeneic LUAD xenografts and human organoid models.
Main Results:
- AVJ16 treatment significantly downregulates pro-oncogenic signaling pathways (Hedgehog, Wnt, PI3K-Akt) by affecting IGF2BP1 RNA binding, RNA, and protein expression.
- AVJ16 inhibits colony formation, invasion, and spheroid growth while enhancing apoptosis and cell death in IGF2BP1-expressing cells.
- AVJ16 prevents tumor growth in LUAD xenografts and induces cell death in IGF2BP1-positive LUAD organoids.
Conclusions:
- AVJ16 effectively inhibits IGF2BP1 function, leading to reduced tumor growth and increased cancer cell death.
- AVJ16 demonstrates significant potential as a targeted therapeutic agent for tumors expressing IGF2BP1.
- This study highlights the therapeutic value of targeting IGF2BP1 in cancer treatment.
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