Evidence map›Paper›PMID 40620540›Full record

ArticleACM-BCB ... ... : the ... ACM Conference on Bioinformatics, Computational Biology and Biomedicine. ACM Conference on Bioinformatics, Computational Biology and Biomedicine2024

New Spatial Phenotypes from Imaging Uncover Survival Differences for Breast Cancer Patients.

Mahmudul Hasan, Ariadna Kim Silva, Shahira Abousamra, Shao-Jun Tang, Prateek Prasanna, Joel Saltz, Kevin Gardner, Chao Chen, Alisa Yurovsky

Abstract read
In one paragraph

Article in ACM-BCB ... ... : the ... ACM Conference on Bioinformatics, Computational Biology and Biomedicine. ACM Conference on Bioinformatics, Computational Biology and Biomedicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Mahmudul HasanStony Brook University, Stony Brook, NY, USA.
Ariadna Kim SilvaStony Brook University, Stony Brook, NY, USA.
Shahira AbousamraStony Brook University, Stony Brook, NY, USA.
Shao-Jun TangStony Brook University, Stony Brook, NY, USA.
Prateek PrasannaStony Brook University, Stony Brook, NY, USA.
Joel SaltzStony Brook University, Stony Brook, NY, USA.
Kevin GardnerColumbia University, New York, NY, USA.
Chao ChenStony Brook University, Stony Brook, NY, USA.
Alisa YurovskyStony Brook University, Stony Brook, NY, USA.

Funding

The linkage between Race, Kaiso and the tumor microenvironment in breast cancer health disparitiesR01CA253368 · NCI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI GARDNER, KEVIN L. · 2020 to 2024
$3.3M
The Role of Kaiso as a predictive breast cancer biomarker in Africa and across the African DiasporaR01CA266040 · NCI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI KEVIN L. GARDNER · 2022 to 2026
$3.1M
Cellular and circuitry mechanisms of NRTI-induced pain pathogenesis in the context of opioids and HIVR01DA057195 · NIDA · STATE UNIVERSITY NEW YORK STONY BROOK · PI SHAO-JUN TANG · 2022 to 2026
$2.5M
SCH: Topological Methods for Breast Tissue QuantificationR01CA297843 · NCI · STATE UNIVERSITY NEW YORK STONY BROOK · PI Chao Chen, Prateek Prasanna · 2024 to 2026
$900k
DMS/NIGMS 1: Topological Study on Histological Images and Spatial TranscriptomicsR01GM148970 · NIGMS · STATE UNIVERSITY NEW YORK STONY BROOK · PI CHEN, CHAO, JOHNSON, TRAVIS STEELE · 2022 to 2024
$682k
IMAT-ITCR Collaboration: Combining FIBI and topological data analysis: Synergistic approaches for tumor structural microenvironment explorationR21CA258493 · NCI · STATE UNIVERSITY NEW YORK STONY BROOK · PI CHEN, CHAO, PRASANNA, PRATEEK · 2022 to 2023
$467k
NCI NIH HHS R01 CA253368NCI NIH HHS R01 CA266040NCI NIH HHS R01 CA297843NCI NIH HHS R21 CA258493NIDA NIH HHS R01 DA057195NIGMS NIH HHS R01 GM148970
6 · The paper itself

Abstract

Imaging technologies have revolutionized the study of the tumor microenvironment (TME) by leveraging spatial analysis, which enables the exploration of tissue organization and cellular communication, as well as aiding cancer diagnosis and prognosis. However, while many advanced spatial analysis methods have been recently published, they are enmeshed with specific imaging technology. An opportunity exists to develop a technology-agnostic methodology that captures complex spatial patterns in the TME as phenotypes to use in downstream tasks. In this paper, we present a novel variation of spatial g-function and a comprehensive imaging-technology-agnostic framework that identifies rich spatial phenotypes that can be used in survival analysis and classification tasks. Applying our methodology to breast cancer, we uncover spatial phenotypes with significance to survival across racial groups and molecular subtypes of breast cancer. We find other phenotypes that are significant to the survival of specific patient categories (such as African American). We also demonstrate that our phenotypes reflect specific biological contexts. These results highlight the relevance of our proposed spatial analysis and phenotype discovery pipeline and demonstrate the benefits of the systematic exploration of spatial phenotypes for more personalized diagnosis and treatments.

Indexed as

Applied computing → Health informaticsCancerComputational proteomicsImagingSpatial PhenotypeSpatial StatisticsSurvival Analysis

Identifiers

PMID40620540
PMCPMC12228512

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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 OpenQuestion graph.