Evidence map›Paper›PMID 28607065›Full record

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

Maintenance of antiangiogenic and antitumor effects by orally active low-dose capecitabine for long-term cancer therapy.

Yin Zhang, Meili Sun, Guichun Huang, Linlin Yin, Qinghua Lai, Yunlong Yang, Xiaoming Xing, Guohua Yu, Yuping Sun, Xinsheng Wang and 3 more

Open access · bronzeAbstract 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 26 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 1 pooled it
1.0field-weighted citation impact, top 25% 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

26 citing papers in PubMed, 1 synthesis or guideline pooled it, 40 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. Article
  5. Article
  6. Article
  7. Tumor biomarkers for diagnosis, prognosis and targeted therapy.Signal transduction and targeted therapy · 2024
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  8. Glucagon Enhances Chemotherapy Efficacy By Inhibition of Tumor Vessels in Colorectal Cancer.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
    Article
  9. Review
  10. Review
  11. Article
  12. Article
  13. Article
  14. A Pilot Study of Peritumor Administration of 5-FU for Preventing Bleeding in Advanced Gastric Cancer.The Korean journal of gastroenterology = Taehan Sohwagi Hakhoe chi · 2022
    Article
  15. Molecular Pathology of Gastric Cancer.Journal of gastric cancer · 2022
    Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

13 authors at 7 institutions in 2 countries.

Yin ZhangCentral Research Laboratory, The Affiliated Hospital of Qingdao University, Qingdao 266071, China.
Meili SunDepartment of Microbiology, Tumor and Cell Biology, Karolinska Institute, 171 77 Stockholm, Sweden.
Guichun HuangDepartment of Microbiology, Tumor and Cell Biology, Karolinska Institute, 171 77 Stockholm, Sweden.
Linlin YinDepartment of Microbiology, Tumor and Cell Biology, Karolinska Institute, 171 77 Stockholm, Sweden.
Qinghua LaiDepartment of Microbiology, Tumor and Cell Biology, Karolinska Institute, 171 77 Stockholm, Sweden.
Yunlong YangDepartment of Microbiology, Tumor and Cell Biology, Karolinska Institute, 171 77 Stockholm, Sweden.
Xiaoming XingCentral Research Laboratory, The Affiliated Hospital of Qingdao University, Qingdao 266071, China.
Guohua YuDepartment of Oncology, Wei Fang People's Hospital, Weifang, Shandong 261041, China.
Yuping SunDepartment of Oncology, Jinan Central Hospital, Shandong University, Jinan, Shandong 250013, China; 13370582181@163.com qdfywxs@163.com nghui@21cn.com yizhi_liu@yahoo.com yihai.cao@ki.se.
Xinsheng WangCentral Research Laboratory, The Affiliated Hospital of Qingdao University, Qingdao 266071, China; 13370582181@163.com qdfywxs@163.com nghui@21cn.com yizhi_liu@yahoo.com yihai.cao@ki.se.
Guohui NieKey Laboratory of International Collaborations, Second People's Hospital of Shenzhen, First Affiliated Hospital of Shenzhen University, Shenzhen 518035, China; 13370582181@163.com qdfywxs@163.com nghui@21cn.com yizhi_liu@yahoo.com yihai.cao@ki.se.
Yizhi LiuState Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-Sen University, Guangzhou 510060, China; 13370582181@163.com qdfywxs@163.com nghui@21cn.com yizhi_liu@yahoo.com yihai.cao@ki.se.
Yihai CaoCentral Research Laboratory, The Affiliated Hospital of Qingdao University, Qingdao 266071, China; 13370582181@163.com qdfywxs@163.com nghui@21cn.com yizhi_liu@yahoo.com yihai.cao@ki.se.
Karolinska Institutet · SEShenzhen Second People's Hospital · CNQingdao University · CNJinan Central Hospital · CNShandong University · CNSun Yat-sen University · CNWeifang People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Long-term uninterrupted therapy is essential for maximizing clinical benefits of antiangiogenic drugs (AADs) in cancer patients. Unfortunately, nearly all clinically available AADs are delivered to cancer patients using disrupted regimens. We aim to develop lifetime, nontoxic, effective, orally active, and low-cost antiangiogenic and antitumor drugs for treatment of cancer patients. Here we report our findings of long-term maintenance therapy with orally active, nontoxic, low cost antiangiogenic chemotherapeutics for effective cancer treatment. In a sequential treatment regimen, robust antiangiogenic effects in tumors were achieved with an anti-VEGF drug, followed by a low-dose chemotherapy. The nontoxic, low dose of the orally active prodrug capecitabine was able to sustain the anti-VEGF-induced vessel regression for long periods. In another experimental setting, maintenance of low-dose capecitabine produced greater antiangiogenic and antitumor effects after AAD plus chemotherapy. No obvious adverse effects were developed after more than 2-mo of consecutive treatment with a low dose of capecitabine. Together, our findings provide a rationalized concept of effective cancer therapy by long-term maintenance of AAD-triggered antiangiogenic effects with orally active, nontoxic, low-cost, clinically available chemotherapeutics.

Indexed as

Neoplasms, ExperimentalNeovascularization, PathologicA549 CellsAdministration, OralAnimalsCapecitabineDrug Screening Assays, AntitumorFemaleHumansHuman Umbilical Vein Endothelial CellsMaleMiceTime FactorsCapecitabineangiogenesiscancer therapychemotherapytumor growthVEGF

Identifiers

PMID28607065
PMCPMC5495268
OpenAlexW2624984899

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.