Drugs targeting SHIP2 demonstrate potent antiproliferative effects irrespective of SHIP2 inhibition

The SH2-containing inositol 5'-phosphatase SHIP2 plays a crucial role in negative regulation of the PI3K/AKT signaling pathway. Putative small molecule inhibitors of SHIP2, AS1949490 and K149 have been reported to elicit a range of beneficial effects in treating or preventing obesity as well as killing cancer cells. However, whether these effects are direct results of SHIP2 inhibition has not been carefully assessed, e.g., in the absence of expression of the protein. Here, we show that these inhibitors alter the PI3K/AKT signaling pathway irrespective of SHIP2 protein expression. Moreover, we found that AS1949490 and K149 alter cell growth in normal and cancer cells lacking both SHIP1 and SHIP2. Overall, our data provide evidence that the antiproliferative effects of AS1949490 and K149 cannot be attributed to SHIP1/2 inhibition.

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Publication Details

Journal
Life Sciences
Published
2024-10-02
DOI
https://doi.org/10.1016/j.lfs.2024.123101
Citations
2
Primary Topic
PI3K/AKT/mTOR signaling in cancer
Type
article
Field-Weighted Citation Impact
0.47

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article

Drugs targeting SHIP2 demonstrate potent antiproliferative effects irrespective of SHIP2 inhibition

Abdelhalim Azzi, Nelson G. M. Gomes, Abdulrahman El Sayed, A Czerwińska
2 citations
Life Sciences
PI3K/AKT/mTOR signaling in cancer
0.47
article

Drugs targeting SHIP2 demonstrate potent antiproliferative effects irrespective of SHIP2 inhibition

Abdelhalim Azzi, Nelson G. M. Gomes, Abdulrahman El Sayed, A Czerwińska
article en
2 citations

Abstract

The SH2-containing inositol 5'-phosphatase SHIP2 plays a crucial role in negative regulation of the PI3K/AKT signaling pathway. Putative small molecule inhibitors of SHIP2, AS1949490 and K149 have been reported to elicit a range of beneficial effects in treating or preventing obesity as well as killing cancer cells. However, whether these effects are direct results of SHIP2 inhibition has not been carefully assessed, e.g., in the absence of expression of the protein. Here, we show that these inhibitors alter the PI3K/AKT signaling pathway irrespective of SHIP2 protein expression. Moreover, we found that AS1949490 and K149 alter cell growth in normal and cancer cells lacking both SHIP1 and SHIP2. Overall, our data provide evidence that the antiproliferative effects of AS1949490 and K149 cannot be attributed to SHIP1/2 inhibition.

Life SciencesVol. 357
Polish Academy of Sciences (PL)
Narodowe Centrum Nauki
Zero hunger
Openalex Percentile: Top 35%
PI3K/AKT/mTOR signaling in cancer
0.47
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Drugs targeting SHIP2 demonstrate potent antiproliferative effects irrespective of SHIP2 inhibition — Abdelhalim Azzi, Nelson G. M. Gomes, et al. · Life Sciences (2024) | TGRS Research Map | TGRS