Evidence map›Paper›PMID 29285203›Full record

ArticleOncology letters2018

Anticancer effect of S-allyl-L-cysteine via induction of apoptosis in human bladder cancer cells.

Jin-Nyoung Ho, Minyong Kang, Sangchul Lee, Jong Jin Oh, Sung Kyu Hong, Sang Eun Lee, Seok-Soo Byun

Open access · diamondAbstract read
In one paragraph

Article in Oncology letters, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
5.6field-weighted citation impact, top 5% 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

11 citing papers in PubMed, 23 citations in OpenAlex.

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  8. Gut bacteria of Varanus salvator possess potential antitumour molecules.International microbiology : the official journal of the Spanish Society for Microbiology · 2021
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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

7 authors at 2 institutions in 1 country.

Jin-Nyoung HoDepartment of Urology, Seoul National University College of Medicine, Seoul National University Bundang Hospital, Seongnam-si, Gyunggi-do 463-707, Republic of Korea.
Minyong KangDepartment of Urology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul 135-710, Republic of Korea.
Sangchul LeeDepartment of Urology, Seoul National University College of Medicine, Seoul National University Bundang Hospital, Seongnam-si, Gyunggi-do 463-707, Republic of Korea.
Jong Jin OhDepartment of Urology, Seoul National University College of Medicine, Seoul National University Bundang Hospital, Seongnam-si, Gyunggi-do 463-707, Republic of Korea.
Sung Kyu HongDepartment of Urology, Seoul National University College of Medicine, Seoul National University Bundang Hospital, Seongnam-si, Gyunggi-do 463-707, Republic of Korea.
Sang Eun LeeDepartment of Urology, Seoul National University College of Medicine, Seoul National University Bundang Hospital, Seongnam-si, Gyunggi-do 463-707, Republic of Korea.
Seok-Soo ByunDepartment of Urology, Seoul National University College of Medicine, Seoul National University Bundang Hospital, Seongnam-si, Gyunggi-do 463-707, Republic of Korea.
Seoul National University Bundang Hospital · KRSamsung Medical Center · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To examine the anticancer effects of S-allyl-L-cysteine (SAC) in human bladder cancer cells and to identify possible molecular mechanisms, bladder cancer cell lines (HTB5, HTB9, JON, UMUC14, T24, and cisplatin resistant-T24R2) were incubated with SAC, and cell proliferation was measured using the Cell Counting Kit-8 assay and clonogenic assay. Cell cycle and apoptosis were evaluated by flow cytometry. Expression levels of apoptosis- and cell cycle-associated proteins were analyzed by western blotting. Proliferation and colony formation in bladder cancer cells was significantly inhibited by SAC treatment in a dose-dependent manner. SAC treatment significantly enhanced apoptosis and promoted a cell cycle arrest in the S phase. SAC also increased the expression of apoptosis-related genes, including caspases, poly (ADP-ribose) polymerase and cytochrome c. SAC had an anticancer effect on bladder cancer cells

Indexed as

anticancerapoptosisbladder cancer cellscell cycleS-allyl-L-cysteine

Identifiers

PMID29285203
PMCPMC5738700
OpenAlexW2765194389

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.