Evidence map›Paper›PMID 29895526›Full record

ArticleEndocrine-related cancer2018

Potent effects of roniciclib alone and with sorafenib against well-differentiated thyroid cancer.

Shu-Fu Lin, Jen-Der Lin, Chuen Hsueh, Ting-Chao Chou, Richard J Wong

Open access · bronzeAbstract read
In one paragraph

Article in Endocrine-related cancer, 2018. 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
0.9field-weighted citation impact, top 24% 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, 11 citations in OpenAlex.

  1. Review
  2. Article
  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

5 authors at 4 institutions in 2 countries.

Shu-Fu LinDepartment of Internal MedicineChang Gung Memorial Hospital, Taoyuan, Taiwan mmg@cgmh.org.tw.
Jen-Der LinDepartment of Internal MedicineChang Gung Memorial Hospital, Taoyuan, Taiwan.
Chuen HsuehChang Gung UniversityTaoyuan, Taiwan.
Ting-Chao ChouLaboratory of Preclinical Pharmacology CoreMemorial Sloan-Kettering Cancer Center, New York, New York, USA.
Richard J WongDepartment of SurgeryMemorial Sloan-Kettering Cancer Center, New York, New York, USA.
Memorial Sloan Kettering Cancer Center · USChang Gung Memorial Hospital · TWChang Gung University · TWNew Jersey Department of Education · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Elisa de Stanchina · 1985 to 2026
$347.4M
NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

Activation of cyclin-dependent kinase activity is frequently observed in many human cancers; therefore, cyclin-dependent kinases that promote cell cycle transition and cell proliferation may be potential targets in the treatment of malignancy. The therapeutic effects of roniciclib, a cyclin-dependent kinase inhibitor for papillary and follicular thyroid cancer (designated as well-differentiated thyroid cancer), were investigated in this study. Roniciclib inhibited cell proliferation in two papillary and two follicular thyroid cancer cell lines in a dose-dependent manner. Roniciclib activated caspase-3 activity and induced apoptosis. Cell cycle progression was arrested in the G2/M phase. Roniciclib treatment

Indexed as

Antineoplastic AgentsApoptosisCaspase 3Cell CycleCell Line, TumorCell ProliferationDose-Response Relationship, DrugHumansPhosphorylationPyrimidinesSignal TransductionSorafenibSulfoxidesThyroid NeoplasmsAntineoplastic AgentsCaspase 3PyrimidinesroniciclibSorafenibSulfoxidescyclin-dependent kinaseroniciclibwell-differentiated thyroid cancer

Identifiers

PMID29895526
PMCPMC7475021
OpenAlexW2808264647

What OpenQuestion holds

Textmetadata
LicenceTDM
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.