Evidence map›Paper›PMID 28784776›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2017

Stress-inducible gene

Yi Seok Chang, Swati P Jalgaonkar, Justin D Middleton, Tsonwin Hai

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 99 papers.

0numbers the graph read from it
0cells of the map it votes in
99citing papers in PubMed
7.7field-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

99 citing papers in PubMed, 155 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Paclitaxel drives TREM2Nature communications · 2026
    Article
  5. Article
  6. Review
  7. Article
  8. Review
  9. New uses of halofuginone to treat cancer.Journal of pharmaceutical analysis · 2025
    Review
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. Review

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

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

4 authors at 1 institution in 1 country.

Yi Seok ChangMolecular, Cellular, and Developmental Biology Program, Ohio State University, Columbus, OH 43210.
Swati P JalgaonkarMolecular, Cellular, and Developmental Biology Program, Ohio State University, Columbus, OH 43210.
Justin D MiddletonMolecular, Cellular, and Developmental Biology Program, Ohio State University, Columbus, OH 43210.
Tsonwin HaiMolecular, Cellular, and Developmental Biology Program, Ohio State University, Columbus, OH 43210; hai.2@osu.edu.
The Ohio State University · US

Funding

Translational Therapeutics Research Program (TT)P30CA016058 · NCI · OHIO STATE UNIVERSITY · PI Tasleem J Padamsee · 1985 to 2026
$132.3M
Ohio State Neuroscience Centr CoreP30NS045758 · NINDS · OHIO STATE UNIVERSITY · PI OBRIETAN, KARL H · 2004 to 2015
$7.7M
NCI NIH HHS P30 CA016058NINDS NIH HHS P30 NS045758
6 · The paper itself

Abstract

Chemotherapy is a double-edged sword. It is anticancer because of its cytotoxicity. Paradoxically, by increasing chemoresistance and cancer metastasis, it is also procancer. However, the underlying mechanisms for chemotherapy-induced procancer activities are not well understood. Here we describe the ability of paclitaxel (PTX), a frontline chemotherapeutic agent, to exacerbate metastasis in mouse models of breast cancer. We demonstrate that, despite the apparent benefit of reducing tumor size, PTX increased the circulating tumor cells in the blood and enhanced the metastatic burden at the lung. At the primary tumor, PTX increased the abundance of the tumor microenvironment of metastasis, a landmark microanatomical structure at the microvasculature where cancer cells enter the blood stream. At the metastatic lung, PTX improved the tissue microenvironment (the "soil") for cancer cells (the "seeds") to thrive; these changes include increased inflammatory monocytes and reduced cytotoxicity. Importantly, these changes in the primary tumor and the metastatic lung were all dependent on

Indexed as

Activating Transcription Factor 3AnimalsAntineoplastic AgentsBreast NeoplasmsCell Line, TumorFemaleGene Expression Regulation, NeoplasticHumansLungLung NeoplasmsMiceNeoplasm MetastasisPaclitaxelStress, PhysiologicalActivating Transcription Factor 3Antineoplastic AgentsAtf3 protein, mousePaclitaxelATF3chemotherapyimmune modulationmetastasisstress response

Identifiers

PMID28784776
PMCPMC5576783
OpenAlexW2744433299

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.