Evidence map›Paper›PMID 28191885›Full record

ArticleNature medicine2017

Molecular definition of a metastatic lung cancer state reveals a targetable CD109-Janus kinase-Stat axis.

Chen-Hua Chuang, Peyton G Greenside, Zoë N Rogers, Jennifer J Brady, Dian Yang, Rosanna K Ma, Deborah R Caswell, Shin-Heng Chiou, Aidan F Winters, Barbara M Grüner and 8 more

Abstract read
In one paragraph

Article in Nature medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 101 papers.

0numbers the graph read from it
0cells of the map it votes in
101citing papers in PubMed
8.4field-weighted citation impact, top 2% of its field
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

101 citing papers in PubMed, 161 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Antagonist nanobodies prevent protease inhibition by CD109.The Journal of biological chemistry · 2026
    Article
  6. Article
  7. Article
  8. Article
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  10. Article
  11. Article
  12. Review
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  14. A STAG2-PAXIP1/PAGR1 axis suppresses lung tumorigenesis.The Journal of experimental medicine · 2025
    Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. Article

41 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

18 authors at 1 institution in 1 country.

Chen-Hua ChuangDepartment of Genetics, Stanford University School of Medicine, Stanford, California, USA.
Peyton G GreensideBiomedical Informatics Training Program, Stanford University School of Medicine, Stanford, California, USA.
Zoë N RogersDepartment of Genetics, Stanford University School of Medicine, Stanford, California, USA.
Jennifer J BradyDepartment of Genetics, Stanford University School of Medicine, Stanford, California, USA.
Dian YangCancer Biology Program, Stanford University School of Medicine, Stanford, California, USA.
Rosanna K MaDepartment of Genetics, Stanford University School of Medicine, Stanford, California, USA.
Deborah R CaswellCancer Biology Program, Stanford University School of Medicine, Stanford, California, USA.
Shin-Heng ChiouDepartment of Genetics, Stanford University School of Medicine, Stanford, California, USA.
Aidan F WintersDepartment of Genetics, Stanford University School of Medicine, Stanford, California, USA.
Barbara M GrünerDepartment of Genetics, Stanford University School of Medicine, Stanford, California, USA.
Gokul RamaswamiDepartment of Genetics, Stanford University School of Medicine, Stanford, California, USA.
Andrew L SpencleyCancer Biology Program, Stanford University School of Medicine, Stanford, California, USA.
Kimberly E KopeckyDepartment of Surgery, Stanford University School of Medicine, Stanford, California, USA.
Leanne C SaylesDepartment of Pediatrics, Stanford University School of Medicine, Stanford, California, USA.
E Alejandro Sweet-CorderoCancer Biology Program, Stanford University School of Medicine, Stanford, California, USA.
Jin Billy LiDepartment of Genetics, Stanford University School of Medicine, Stanford, California, USA.ORCID http://orcid.org/0000-0003-0713-1399
Anshul KundajeDepartment of Genetics, Stanford University School of Medicine, Stanford, California, USA.
Monte M WinslowDepartment of Genetics, Stanford University School of Medicine, Stanford, California, USA.
Stanford University · US

Funding

Translational Oncology Research Program (Project-005)P30CA124435 · NCI · STANFORD UNIVERSITY · PI Melinda L. Telli · 2007 to 2026
$71.4M
POSTDOCTORAL TRAINING IN MEDICAL INFORMATION SCIENCEST15LM007033 · NLM · STANFORD UNIVERSITY · PI SYLVIA KATINA PLEVRITIS · 1985 to 2026
$25.5M
Leveraging innovative technologies in basic and clinical cancer researchT32CA009302 · NCI · STANFORD UNIVERSITY · PI LAURA D ATTARDI, Aaron M Newman · 1985 to 2026
$19.1M
Profiling and Dissecting the Dynamic Regulation of RNA EditingR01GM102484 · NIGMS · STANFORD UNIVERSITY · PI LI, JIN BILLY · 2013 to 2021
$3.1M
Molecular Dissection of an Arntl2 induced pro-metastatic secretomeR01CA204620 · NCI · STANFORD UNIVERSITY · PI WINSLOW, MONTE MEIER · 2016 to 2020
$1.8M
Molecular Dissection of Lung Cancer Progression and MetastasisR01CA175336 · NCI · STANFORD UNIVERSITY · PI WINSLOW, MONTE MEIER · 2013 to 2017
$1.7M
Mechanisms of chemotherapy response and tumor re-initiation in lung cancerR01CA157510 · NCI · STANFORD UNIVERSITY · PI SWEET-CORDERO, ERIC ALEJANDRO · 2011 to 2015
$1.7M
Mechanisms governing tumor differentiation and metastasisF32CA189659 · NCI · STANFORD UNIVERSITY · PI BRADY, JENNIFER · 2014 to 2015
$106k
NCI NIH HHS F32 CA189659NCI NIH HHS P30 CA124435NCI NIH HHS R01 CA157510NCI NIH HHS R01 CA175336NCI NIH HHS R01 CA204620NCI NIH HHS T32 CA009302NIGMS NIH HHS R01 GM102484NLM NIH HHS T15 LM007033
6 · The paper itself

Abstract

Lung cancer is the leading cause of cancer deaths worldwide, with the majority of mortality resulting from metastatic spread. However, the molecular mechanism by which cancer cells acquire the ability to disseminate from primary tumors, seed distant organs, and grow into tissue-destructive metastases remains incompletely understood. We combined tumor barcoding in a mouse model of human lung adenocarcinoma with unbiased genomic approaches to identify a transcriptional program that confers metastatic ability and predicts patient survival. Small-scale in vivo screening identified several genes, including Cd109, that encode novel pro-metastatic factors. We uncovered signaling mediated by Janus kinases (Jaks) and the transcription factor Stat3 as a critical, pharmacologically targetable effector of CD109-driven lung cancer metastasis. In summary, by coupling the systematic genomic analysis of purified cancer cells in distinct malignant states from mouse models with extensive human validation, we uncovered several key regulators of metastatic ability, including an actionable pro-metastatic CD109-Jak-Stat3 axis.

Indexed as

AdenocarcinomaAnimalsAntigens, CDBlotting, WesternCell Line, TumorDisease Models, AnimalGene Expression Regulation, NeoplasticGene Knockdown TechniquesJanus Kinase 1Janus Kinase 3Janus KinasesLung NeoplasmsMiceMolecular Targeted TherapyNeoplasm MetastasisNeoplasm ProteinsAntigens, CDCD109 protein, mouseHras protein, mouseJak1 protein, mouseJak3 protein, mouseJanus Kinase 1Janus Kinase 3Janus KinasesNeoplasm ProteinsProtein Kinase InhibitorsProto-Oncogene Proteins p21(ras)Stat3 protein, mouseSTAT3 Transcription FactorTumor Suppressor Protein p53

Identifiers

PMID28191885
PMCPMC6453542
OpenAlexW2588755013

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.