Unknown,Transcriptomics,Genomics,Proteomics

Dataset Information

0

Transcription profiling of human A549 lung cancer cells treated with compounds from a series of inhibitors developed against the human LIM kinases LIMK1 and LIMK2


ABSTRACT: To investigate an unknown mechanism of cytotoxicity, A549 human lung-cancer cells were treated with compounds from a series of inhibitors developed against the human LIM kinases LIMK1 and LIMK2. Compounds 1 and 2 inhibit LIM kinase activity in vitro and affect cell proliferation and survival in vivo. Compounds 3 and 4 inhibit LIM kinases but do not affect cell survival or proliferation. Compounds 5 and 6 affect proliferation and survival but do not inhibit LIM kinases. Nocodazole was included as a comparator because the compounds were known to affect microtubule stability. A treatment of 7 hours was used to examine events prior to apoptosis, while the dose levels captured both cytotoxicity and inhibition of LIMKs (Compounds 1 and 2), LIMK inhibition alone ( Compounds 3 and 4) or cytotoxicity alone (Compounds 5, 6, and Nocodazole).

ORGANISM(S): Homo sapiens

SUBMITTER: Heshani Desilva 

PROVIDER: E-TABM-450 | biostudies-arrayexpress |

REPOSITORIES: biostudies-arrayexpress

altmetric image

Publications


In developing inhibitors of the LIM kinases, the initial lead molecules combined potent target inhibition with potent cytotoxic activity. However, as subsequent compounds were evaluated, the cytotoxic activity separated from inhibition of LIM kinases. A rapid determination of the cytotoxic mechanism and its molecular target was enabled by integrating data from two robust core technologies. High-content assays and gene expression profiling both indicated an effect on microtubule stability. Althou  ...[more]

Similar Datasets

2005-08-20 | E-MEXP-401 | biostudies-arrayexpress
| PRJNA633869 | ENA
2009-09-12 | E-GEOD-17353 | biostudies-arrayexpress
2018-12-19 | PXD010167 | Pride
2012-06-28 | E-GEOD-39002 | biostudies-arrayexpress
2012-06-29 | GSE39002 | GEO
2021-03-25 | PXD015468 | Pride
2023-03-11 | PXD024999 | Pride
| PRJNA1052015 | ENA
2021-11-18 | GSE185596 | GEO