Evidence map›Paper›PMID 40613036›Full record

ArticleOncology letters2025

BLID is a drug-responsive target of FOXO3a and multi-omics analysis reveals survival mechanisms and therapeutic vulnerabilities in BLID-deficient breast cancer cells.

Sivaramakrishna Yadavalli, Rong Hu, Antonina Rait, Rency Varghese, James Li, Ofer Eidelman, Xiaojun Zou, Habtom Ressom, Esther Chang, Meera Srivastava and 2 more

Abstract read
In one paragraph

Article in Oncology letters, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

12 authors.

Sivaramakrishna YadavalliGeorgetown Lombardi Comprehensive Cancer Center, Georgetown University Medical Center, Washington, DC 20057, USA.
Rong HuGeorgetown Lombardi Comprehensive Cancer Center, Georgetown University Medical Center, Washington, DC 20057, USA.
Antonina RaitGeorgetown Lombardi Comprehensive Cancer Center, Georgetown University Medical Center, Washington, DC 20057, USA.
Rency VargheseGeorgetown Lombardi Comprehensive Cancer Center, Georgetown University Medical Center, Washington, DC 20057, USA.
James LiGeorgetown Lombardi Comprehensive Cancer Center, Georgetown University Medical Center, Washington, DC 20057, USA.
Ofer EidelmanUniformed Services University of Health Sciences, Bethesda, MD 20814, USA.
Xiaojun ZouGeorgetown Lombardi Comprehensive Cancer Center, Georgetown University Medical Center, Washington, DC 20057, USA.
Habtom RessomGeorgetown Lombardi Comprehensive Cancer Center, Georgetown University Medical Center, Washington, DC 20057, USA.
Esther ChangGeorgetown Lombardi Comprehensive Cancer Center, Georgetown University Medical Center, Washington, DC 20057, USA.
Meera SrivastavaUniformed Services University of Health Sciences, Bethesda, MD 20814, USA.
Robert ClarkeGeorgetown Lombardi Comprehensive Cancer Center, Georgetown University Medical Center, Washington, DC 20057, USA.
Usha KasidGeorgetown Lombardi Comprehensive Cancer Center, Georgetown University Medical Center, Washington, DC 20057, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BH-3 like motif containing inducer of cell death (BLID) is a known prognostic factor in breast cancer. The aim of the present study was to determine the significance of BLID in the outcomes of chemotherapy and mechanisms affected in BLID-deficient breast cancer cells. Reverse transcription-PCR, reverse transcription-quantitative PCR, dual-luciferase reporter and chromatin immunoprecipitation assays were used to determine the effects of drugs on BLID expression and binding of forkhead box protein O3a (FOXO3a) to the BLID promoter. RNA arrays, antibody microarrays and microRNA arrays were used to illuminate the omics features of BLID knockdown vs. isogenic control breast cancer cell lines. Kaplan-Meier plotter and receiver operating characteristic plotter tools were used to determine the prognostic and therapy response benefits of BLID expression using publicly available clinical datasets. BLID expression was induced in response to several chemotherapeutic drugs. Drug treatment resulted in increased binding of FOXO3a to the BLID promoter, and FOXO3a knockdown was associated with decreased expression of BLID. BLID depletion led to a decrease in the cytotoxicity of chemotherapeutic drugs. Through multi-omics profiling, three functionally distinct classes of effectors that were predominately influenced in BLID knockdown cells were identified: i) Genes and proteins associated with cell death and survival, including cellular inhibitor of apoptosis protein 2/baculoviral IAP repeat containing 3, phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit α/p110α and DFNA5/gasdermin E; ii) members of the aldo-ketoreductase family 1, specifically aldo-keto reductase family 1 member C3 implicated in drug metabolism; and iii) effectors of the interferon response, including IFNβ1, interferon-induced protein with tetratricopeptide repeats 2 and interferon-induced protein with tetratricopeptide repeats 3. Finally, higher BLID expression was associated with improved overall survival in several types of cancer and the response of breast cancer to anthracyclines. The results of the present study demonstrated that BLID is a target of FOXO3a, and BLID-deficiency in breast cancer cells was associated with modulation of cell death, survival and proliferation, chemoresistance, drug potency, and the interferon response. These findings highlighted BLID as a promising biomarker of drug response and offer a novel framework of integrative mechanisms of therapeutic resistance and disease progression.

Indexed as

5-bisphosphate 3-kinase catalytic subunit αaldo-keto reductase family 1 member C3BH-3 like motif containing inducer of cell deathbreast cancercellular inhibitor of apoptosis protein 2chemosensitivityDFNA5forkhead box protein O3ainterferonsmulti-omicsphosphatidylinositol-4

Identifiers

PMID40613036
PMCPMC12217432

What Socratic holds

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.