Cell fitness is an omniphenotype
Jacobs, N. C.; Park, J.; Peterson, T.
Show abstract
Moores law states that computers get faster and less expensive over time. In contrast in biopharma, there is the reverse spelling, Erooms law, which states that drug discovery is getting slower and costing more money every year. Herein, we propose a solution to this problem. We put forth a consensus algorithm for inexpensively and rapidly prioritizing new factors of interest (e.g., a gene or drug) in human disease research. Specifically, we argue for synthetic interaction testing in mammalian cells using cell fitness - which reflect changes in cell number that could be due many effects - as a readout to judge the potential of the new factor. That is, if we combine perturbing a known factor with perturbing an unknown factor and they produce a synergistic, i.e., multiplicative rather than additive cell fitness phenotype, this justifies proceeding with the unknown gene/drug in more complex models where the known perturbation is already validated. This recommendation is backed by the following evidence we demonstrate herein: 1) human genes currently known to be important to cell fitness involve nearly all classifications of cellular and molecular processes; 2) Nearly all human genes important in cancer - a disease defined by altered cell number - are also important in other common diseases; 3) Many drugs affect a patients condition and the fitness of their cells comparably. We provide proof of concept of the Omniphenotype model using the widely used osteoporosis drug, bisphosphonates, implicating its mechanism of action (MoA) genes, ATRAID, SLC37A3, and FDPS, as potential gerotargets for neurodegenerative conditions. Taken together, these findings suggest cell fitness could be a broadly applicable phenotype for understanding gene, disease, and drug function. Measuring cell fitness is robust and requires little time and money. These are features that have long been capitalized on by pioneers using model organisms that we hope more mammalian biologists will recognize. Short summaryCell fitness is a biological hash function that enables interoperability of biomedical data.
Matching journals
The top 8 journals account for 50% of the predicted probability mass.
Similar papers in this journal
- An unsupervised feature extraction and selection strategy for identifying epithelial-mesenchymal transition state metrics in breast cancer and melanoma 92%
- Cooperative RNA degradation stabilizes intermediate epithelial-mesenchymal states and supports a phenotypic continuum 92%
- Functional impact of the hyperduplication genomophenotype in high copy number endometrial cancer 92%
Similar papers in this journal
- MOATAI-VIR - an AI algorithm that predicts severe adverse events and molecular features for COVID-19’s complications 94%
- Genome-wide investigation of gene-cancer associations for the prediction of novel therapeutic targets in oncology 93%
- ATP signaling in the integrative neural center of Aplysia californica 91%
Similar papers in this journal
Similar papers in this journal
- Spike-in normalization for single-cell RNA-seq reveals dynamic global transcriptional activity mediating anti-cancer drug response 95%
- Identifying essential genes across eukaryotes by machine learning 94%
- Prognostic importance of splicing-triggered aberrations of protein complex interfaces in cancer 93%
Similar papers in this journal
- RAF conformational autoinhibition and 14-3-3 proteins promote paradoxical activation 94%
- De novo identification of universal cell mechanics gene signatures 92%
- Systematic genetic characterization of the human PKR kinase domain highlights its functional malleability to escape a poxvirus substrate mimic 92%
"Similar papers" are the closest papers from that journal in the model's embedding space. They show what the match is built on, but the ranking comes mostly from a classifier over the whole training set, not from these examples alone.