Evidence map›Paper›PMID 38773085›Full record

ArticleNature communications2024

Integrative multi-region molecular profiling of primary prostate cancer in men with synchronous lymph node metastasis.

Udit Singhal, Srinivas Nallandhighal, Jeffrey J Tosoian, Kevin Hu, Trinh M Pham, Judith Stangl-Kremser, Chia-Jen Liu, Razeen Karim, Komal R Plouffe, Todd M Morgan and 12 more

Abstract read
In one paragraph

Article in Nature communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

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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

22 authors.

Udit Singhal *Department of Urology, Michigan Medicine, Ann Arbor, MI, USA. usinghal@med.umich.edu.ORCID http://orcid.org/0000-0002-3928-9476
Srinivas Nallandhighal *Department of Urology, Michigan Medicine, Ann Arbor, MI, USA.ORCID http://orcid.org/0000-0002-9227-0168
Jeffrey J TosoianDepartment of Urology, Vanderbilt University, Nashville, TN, USA.ORCID http://orcid.org/0000-0002-7614-9931
Kevin HuDepartment of Pathology, Michigan Medicine, Ann Arbor, MI, USA.
Trinh M PhamDepartment of Urology, Michigan Medicine, Ann Arbor, MI, USA.
Judith Stangl-KremserDepartment of Urology, Michigan Medicine, Ann Arbor, MI, USA.
Chia-Jen LiuCollege of Literature, Science, and Arts, University of Michigan, Ann Arbor, MI, USA.
Razeen KarimCollege of Literature, Science, and Arts, University of Michigan, Ann Arbor, MI, USA.
Komal R PlouffeMichigan Center for Translational Pathology, Michigan Medicine, Ann Arbor, MI, USA.
Todd M MorganDepartment of Urology, Michigan Medicine, Ann Arbor, MI, USA.ORCID http://orcid.org/0000-0002-1140-0603
Marcin CieslikRogel Cancer Center, Michigan Medicine, Ann Arbor, MI, USA.
Roberta LucianòDepartment of Pathology, Universita Vita-Salute San Raffaele, Milan, Italy.
Shahrokh F ShariatDepartment of Urology, Medical University of Vienna, Vienna, Austria.
Nadia FinocchioDepartment of Urology, Universita Vita-Salute San Raffaele, Milan, Italy.
Lucia DambrosioDepartment of Urology, Universita Vita-Salute San Raffaele, Milan, Italy.
Claudio DoglioniDepartment of Pathology, Universita Vita-Salute San Raffaele, Milan, Italy.ORCID http://orcid.org/0000-0002-4969-5216
Arul M ChinnaiyanDepartment of Urology, Michigan Medicine, Ann Arbor, MI, USA.ORCID http://orcid.org/0000-0001-9282-3415
Scott A TomlinsDepartment of Pathology, Michigan Medicine, Ann Arbor, MI, USA.
Alberto BrigantiDepartment of Urology, Universita Vita-Salute San Raffaele, Milan, Italy.
Ganesh S PalapattuDepartment of Urology, Michigan Medicine, Ann Arbor, MI, USA.ORCID http://orcid.org/0000-0002-9520-0480
Aaron M UdagerRogel Cancer Center, Michigan Medicine, Ann Arbor, MI, USA. udager@med.umich.edu.ORCID http://orcid.org/0000-0002-8254-5404
Simpa S SalamiDepartment of Urology, Michigan Medicine, Ann Arbor, MI, USA. simpa@med.umich.edu.ORCID http://orcid.org/0000-0001-7461-7079

Funding

XenograftP30CA046592 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Alexey I Nesvizhskii · 1988 to 2026
$178.2M
Tissue/InformaticsP50CA186786 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Ganesh S Palapattu · 2014 to 2026
$27.6M
Michigan-VUMC Biomarker Characterization CenterU2CCA271854 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ARUL M CHINNAIYAN · 2022 to 2026
$5.4M
Discovery and qualification of transcriptomic biomarkers for the early detection of aggressive prostate cancerU01CA214170 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI CHINNAIYAN, ARUL M · 2016 to 2021
$3.3M
Exploiting drivers of androgen receptor signaling negative prostate cancer for prR01CA183857 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI TOMLINS, SCOTT A · 2014 to 2018
$1.6M
Defining the Biological Arc of Grade Group 1 Prostate CancerR37CA283857 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Simpa Samuel Salami · 2023 to 2026
$1.4M
NCI NIH HHS L30 CA264387NCI NIH HHS P30 CA046592NCI NIH HHS P50 CA186786NCI NIH HHS R01 CA183857NCI NIH HHS R37 CA283857NCI NIH HHS U01 CA214170NCI NIH HHS U2C CA271854
6 · The paper itself

Abstract

Localized prostate cancer is frequently composed of multiple spatially distinct tumors with significant inter- and intra-tumoral molecular heterogeneity. This genomic diversity gives rise to many competing clones that may drive the biological trajectory of the disease. Previous large-scale sequencing efforts have focused on the evolutionary process in metastatic prostate cancer, revealing a potential clonal progression to castration resistance. However, the clonal origin of synchronous lymph node (LN) metastases in primary disease is still unknown. Here, we perform multi-region, targeted next generation sequencing and construct phylogenetic trees in men with prostate cancer with synchronous LN metastasis to better define the pathologic and molecular features of primary disease most likely to spread to the LNs. Collectively, we demonstrate that a combination of histopathologic and molecular factors, including tumor grade, presence of extra-prostatic extension, cellular morphology, and oncogenic genomic alterations are associated with synchronous LN metastasis.

Indexed as

Lymphatic MetastasisProstatic NeoplasmsAgedHigh-Throughput Nucleotide SequencingHumansLymph NodesMaleMiddle AgedNeoplasm GradingPhylogeny

Identifiers

PMID38773085
PMCPMC11109137

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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.