Evidence map›Paper›PMID 42065041›Full record

ReviewOncology research2026

AI-Guided Discovery of Oncogenic Signaling Crosstalk in Tumor Progression and Drug Resistance.

Edward Sutanto, Rinni Sutanto, Sara Velichkovikj, Nikola Hadzi-Petrushev, Mitko Mladenov, Dimiter Avtanski, Radoslav Stojchevski

Abstract readReview
In one paragraph

Review in Oncology research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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

7 authors.

Edward SutantoCUNY School of Medicine, The City College of New York, New York, NY, USA.
Rinni SutantoNew York Institute of Technology College of Osteopathic Medicine, Glen Head, NY, USA.
Sara VelichkovikjOffice of Clinical Research, Lenox Hill Hospital, Northwell Health, New York, NY, USA.
Nikola Hadzi-PetrushevFaculty of Natural Sciences and Mathematics, Institute of Biology, Ss. Cyril and Methodius University, Skopje, North Macedonia.
Mitko MladenovFaculty of Natural Sciences and Mathematics, Institute of Biology, Ss. Cyril and Methodius University, Skopje, North Macedonia.
Dimiter AvtanskiFriedman Diabetes Institute, Lenox Hill Hospital, Northwell Health, New York, NY, USA.
Radoslav StojchevskiFriedman Diabetes Institute, Lenox Hill Hospital, Northwell Health, New York, NY, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The rapid growth and accessibility of artificial intelligence (AI) and machine learning (ML) have opened many avenues to revolutionize biomedical research, particularly in oncogenesis. Oncogenesis is a hallmark process in the development of cancer, involving the amplification of proto-oncogenes and the subsequent dysregulation of molecular signaling networks. These pathways-including the RAS/RAF/MEK/ERK, PI3K-AKT, JAK-STAT, TGF-β/Smad, Wnt/β-Catenin, and Notch cascades-have been studied extensively in isolation, with major strides achieved in understanding how they drive cancer. However, there are still many considerations regarding how these networks interact. Ongoing studies show that crosstalk among these pathways occurs through feedback loops, shared intermediates, and compensatory activation, creating a complex network that enables tumor cells to adapt and metastasize. New developments in AI and ML have enabled modeling and prediction of these interactions for pathway discovery, mapping oncogenic crosstalk, predicting drug resistance and therapeutic responses, and complex data analysis. Novel technologies such as feature selection algorithms and convolutional neural networks have demonstrated immense translational potential to bridge computational predictions in cancer genomics with clinical applications. Similar models have also proven useful for learning from genomic datasets and reducing multidimensionality in heterogeneous multiomics data. As current AI/ML approaches continue to develop, it is also important to consider the limitations of batch effects, model generalizability, and potential bias in training datasets. This review aims to integrate the most recent AI and ML applications in uncovering the hidden interactions within oncogenic networks that drive tumorigenesis, heterogeneity, and resistance to therapies. Moreover, this review aims to synthesize the functionality of emerging computational methods that elucidate these insights, as well as the transformative implications of AI-guided systems biology on precision oncology and combinatorial therapies.

Indexed as

Artificial IntelligenceCarcinogenesisDrug Resistance, NeoplasmNeoplasmsSignal TransductionAnimalsDisease ProgressionHumansMachine LearningOncogenesArtificial intelligencedrug resistancemachine learningneural networksoncogenic signaling pathwaystumor progression

Identifiers

PMID42065041
PMCPMC13126398

What OpenQuestion holds

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Registered trials

None linked

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.