Evidence map›Paper›PMID 28356899›Full record

ReviewThe Yale journal of biology and medicine2017

Drug Development Against Metastatic Cancers.

Chen Wang, Sui Huang

Open access · greenAbstract readReview
In one paragraph

Review in The Yale journal of biology and medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.7field-weighted citation impact, top 29% 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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Review
  2. Novel insights into the role of aptamers in the fight against cancer.Journal of cancer research and clinical oncology · 2019
    Review
  3. Article
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

2 authors at 1 institution in 1 country.

Chen WangDepartment of Cell and Molecular Biology, Northwestern University, Feinberg School of Medicine, Chicago, IL.
Sui HuangDepartment of Cell and Molecular Biology, Northwestern University, Feinberg School of Medicine, Chicago, IL.
Northwestern University · US

Funding

Tumor Environment and Metastasis (TEAM) Research ProgramP30CA060553 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Daniela E Matei · 1993 to 2026
$153.9M
The Structure and Function of Perinucleolar CompartmentR01GM078555 · NIGMS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI HUANG, SUI · 2007 to 2015
$2.6M
NCI NIH HHS P30 CA060553NIGMS NIH HHS R01 GM078555
6 · The paper itself

Abstract

While combinational diagnostic and treatment strategies over the past decades have significantly improved the overall survival of cancer patients, metastatic cancer remains a leading cause of death in developed countries. The lack of successful treatment strategies for the disease is in large part due to the complexity of the metastatic transformation, which embodies extensive cellular and extracellular alterations, enabling metastatic cancer cells to reach and colonize other organs. The mode of action for the majority of anti-cancer drugs used in clinics today is primarily tumor growth inhibition. While they are effective in destroying cancer cells, they fall short in blocking metastasis. Here we discuss the evolution of past and current anti-cancer drug development, the limits of current strategies, and possible alternative approaches for future drug development against metastatic cancers.

Indexed as

AnimalsAntineoplastic AgentsHumansNeoplasm MetastasisNeoplasmsAntineoplastic Agentsanti-cancer drugsanti-metastasismetastasistreatment strategies

Identifiers

PMID28356899
PMCPMC5369029
OpenAlexW2735425055

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.