Sabutoclax

response biomarkers — cross-omics
Drug responseDRUG → MUTATIONCell lineBI-97C1

Across CCLE and GDSC cell-line panels, response to Sabutoclax is significantly associated with the mutation status of multiple genes, with LARGE_INTESTINE cell lines showing a particularly strong set of associations.

The most reproducible Sabutoclax response-associated genes across cancer lineages are JMJD1C, SPEG, and CSMD2, each associated with drug response in up to 4 lineages. Since the analysis identifies associations rather than directional relationships, both response-to-biomarker and biomarker-to-response views are provided.

Each biomarker is linked to its corresponding Q-omics profile. The box plot shows the strongest observed association, Sabutoclax response grouped by JMJD1C status in LARGE_INTESTINE.

Mutation status biomarkers of Sabutoclax response

Ranked by combined sampling and lineage consensus. X-score (response→biomarker) and Y-score (biomarker→response) are standardized regression coefficients; both directions are reported because the association is undirected. The reported p-values are derived from the association test.
LineagePartner geneX-scoreY-scorep(X)p(Y)Sampling consensusLineage consensus
LARGE_INTESTINEJMJD1C →+1.999+0.384.036.01333
BLOOD_LeukemiaSPEG →+3.169+0.368.013.01524
LARGE_INTESTINECSMD2 →+1.263+0.325.031.03133
LARGE_INTESTINEMUC4 →+0.769+0.404.031.00933
BLOOD_LeukemiaANK3 →+2.807+0.323.042.01833
LUNG_NSCLC_LUADSPTBN5 →+1.914+0.376.046.04632
Each biomarker links to its Q-omics profile. Showing the 6 strongest associations by consensus.

Sabutoclax response by JMJD1C status — LARGE_INTESTINE

Box plot of Sabutoclax response in JMJD1C-mutant vs wild-type cell lines in LARGE_INTESTINE.

Explore this box plot interactively →

Exploration