Evidence map›Paper›PMID 30404185›Full record

ArticleMolecules (Basel, Switzerland)2018

Novel Rhodanine Derivative, 5-[4-(4-Fluorophenoxy) phenyl]methylene-3-{4-[3-(4-methylpiperazin-1-yl) propoxy]phenyl}-2-thioxo-4-thiazolidinone dihydrochloride, Induces Apoptosis via Mitochondria Dysfunction and Endoplasmic Reticulum Stress in Human Colon Cancer Cells.

Hye-Uk Jung, Jeong-Hun Lee, Kyung-Sook Chung, Joo Young Hong, Jung-Hye Choi, Soo-Dong Kim, Eun Joo Roh, Kye Jung Shin, Kyung-Tae Lee

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.2field-weighted citation impact, top 46% 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

0 citing papers in PubMed, 6 citations in OpenAlex.

No citing paper in PubMed yet.

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

9 authors at 4 institutions in 1 country.

Hye-Uk JungDepartment of Pharmaceutical Biochemistry, College of Pharmacy, Kyung Hee University, Seoul 130-701, Korea. 1109jhuk@naver.com.
Jeong-Hun LeeDepartment of Pharmaceutical Biochemistry, College of Pharmacy, Kyung Hee University, Seoul 130-701, Korea. ztztzt08@hanmail.net.
Kyung-Sook ChungDepartment of Pharmaceutical Biochemistry, College of Pharmacy, Kyung Hee University, Seoul 130-701, Korea. adella76@hanmail.net.
Joo Young HongDepartment of Pharmaceutical Biochemistry, College of Pharmacy, Kyung Hee University, Seoul 130-701, Korea. hjisuk1206@naver.com.
Jung-Hye ChoiDepartment of Life and Nanopharmaceutical Science, Graduate School, Kyung Hee University, Seoul 130-701, Korea. jchoi@khu.ac.kr.
Soo-Dong KimDepartment of Urology, College of Medicine, Dong-A University, Pusan 602-715, Korea. rose1508@naver.com.
Eun Joo RohLife/Health Division, Korea Institute of Science and Technology, 5Wolsong-gil, Seongbuk-gu, Seoul 136-791, Korea. heesu3620@hanmail.net.
Kye Jung ShinIntegrated Research Institute of Pharmaceutical Sciences, College of Pharmacy, The Catholic University of Korea, 43 Jibong-ro, Wonmi-gu, Bucheon, Gyeonggi-do 420-743, Korea. kyejung@catholic.ac.kr.
Kyung-Tae LeeDepartment of Pharmaceutical Biochemistry, College of Pharmacy, Kyung Hee University, Seoul 130-701, Korea. ktlee@khu.ac.kr.ORCID 0000-0002-3141-3727
Kyung Hee University · KRCatholic University of Korea · KRDong-A University · KRKorea Institute of Science and Technology · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We previously reported that 5-[4-(4-fluorophenoxy) phenyl] methylene-3-{4-[3-(4-methylpiperazin-1-yl)propoxy]phenyl}-2-thioxo-4-thiazolidinone dihydrochloride (KSK05104) has potent, selective and metabolically stable IKKβ inhibitory activities. However, the apoptosis-inducing of KSK05104 and its underlying mechanism have not yet been elucidated in human colon cancer cells. We show that KSK05104 triggered apoptosis, as indicated by externalization of Annexin V-targeted phosphatidylserine residues in HT-29 and HCT-116 cells. KSK05104 induced the activation of caspase-8, -9, and -3, and the cleavage of poly (ADP ribose) polymerase-1 (PARP-1). KSK05104-induced apoptosis was significantly suppressed by pretreatment with z-VAD-fmk (a broad caspase inhibitor). KSK05104 also induced release of cytochrome

Indexed as

Antineoplastic AgentsApoptosisCalciumCell Line, TumorColonic NeoplasmsEndoplasmic ReticulumEndoplasmic Reticulum StressHCT116 CellsHT29 CellsHumansMembrane Potential, MitochondrialMitochondriaRhodanineAntineoplastic AgentsCalciumRhodanineapoptosiscalciumcolon cancerER stressmitochondriarhodanine derivative

Identifiers

PMID30404185
PMCPMC6278386
OpenAlexW2899540799

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.