Evidence map›Paper›PMID 39642223›Full record

ArticleScience advances2024

Charting the transcriptomic landscape of primary and metastatic cancers in relation to their origin and target normal tissues.

Neel Sanghvi, Camilo Calvo-Alcañiz, Padma S Rajagopal, Stefano Scalera, Valeria Canu, Sanju Sinha, Fiorella Schischlik, Kun Wang, Sanna Madan, Eldad Shulman and 4 more

Abstract read
In one paragraph

Article in Science advances, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

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  12. The Dynamic Landscape of the Coagulome of Metastatic Malignant Melanoma.International journal of molecular sciences · 2025
    Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors.

Neel SanghviCancer Data Science Laboratory (CDSL), National Cancer Institute (NCI), National Institutes of Health (NIH), Bethesda, MD, USA.ORCID 0000-0003-2929-3401
Camilo Calvo-AlcañizCancer Data Science Laboratory (CDSL), National Cancer Institute (NCI), National Institutes of Health (NIH), Bethesda, MD, USA.
Padma S RajagopalCancer Data Science Laboratory (CDSL), National Cancer Institute (NCI), National Institutes of Health (NIH), Bethesda, MD, USA.ORCID 0000-0002-0489-0819
Stefano ScaleraTranslational Oncology Research Unit, IRCSS Regina Elena National Cancer Institute, Via Elio Chianesi, Rome, Italy.ORCID 0000-0001-5192-5917
Valeria CanuTranslational Oncology Research Unit, IRCSS Regina Elena National Cancer Institute, Via Elio Chianesi, Rome, Italy.ORCID 0000-0001-9085-7320
Sanju SinhaCancer Data Science Laboratory (CDSL), National Cancer Institute (NCI), National Institutes of Health (NIH), Bethesda, MD, USA.ORCID 0000-0002-2688-0603
Fiorella SchischlikCancer Data Science Laboratory (CDSL), National Cancer Institute (NCI), National Institutes of Health (NIH), Bethesda, MD, USA.
Kun WangCancer Data Science Laboratory (CDSL), National Cancer Institute (NCI), National Institutes of Health (NIH), Bethesda, MD, USA.ORCID 0000-0001-8923-8557
Sanna MadanCancer Data Science Laboratory (CDSL), National Cancer Institute (NCI), National Institutes of Health (NIH), Bethesda, MD, USA.
Eldad ShulmanCancer Data Science Laboratory (CDSL), National Cancer Institute (NCI), National Institutes of Health (NIH), Bethesda, MD, USA.ORCID 0000-0002-1859-8819
Antonios Papanicolau-SengosLaboratory of Pathology, National Cancer Institute (NCI), National Institutes of Health (NIH), Bethesda, MD, USA.ORCID 0009-0008-9276-7052
Giovanni BlandinoTranslational Oncology Research Unit, IRCSS Regina Elena National Cancer Institute, Via Elio Chianesi, Rome, Italy.
Eytan RuppinCancer Data Science Laboratory (CDSL), National Cancer Institute (NCI), National Institutes of Health (NIH), Bethesda, MD, USA.ORCID 0000-0002-7862-3940
Nishanth Ulhas NairCancer Data Science Laboratory (CDSL), National Cancer Institute (NCI), National Institutes of Health (NIH), Bethesda, MD, USA.ORCID 0000-0002-8832-0329

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Metastasis is a leading cause of cancer-related deaths, yet understanding how metastatic tumors adapt from their origin to their target tissues remains a fundamental challenge. To address this, we assessed whether primary and metastatic tumors more closely resemble their tissues of origin or target tissues in terms of gene expression. We analyzed expression profiles from multiple cancer types and normal tissues, including single-cell and bulk RNA sequencing data from both paired and unpaired patient cohorts. Primary tumors were overall more transcriptomically similar to their tissues of origin, while metastases shifted toward their target tissues. However, pathway-level analysis highlighted critical metabolic and immune transcriptomic changes toward target tissues during metastasis in both primary and metastatic tumors. In addition, primary tumors exhibited higher activity in cancer hallmarks such as "Activating Invasion and Metastasis" when compared to metastases. This comprehensive analysis provides a transcriptome-wide view of the processes through which cancer tumors adapt to their metastatic environments before and after metastasis.

Indexed as

Gene Expression ProfilingGene Expression Regulation, NeoplasticNeoplasm MetastasisNeoplasmsTranscriptomeHumans

Identifiers

PMID39642223
PMCPMC11623296

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Registered trials

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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.