Evidence map›Paper›PMID 27068261›Full record

ArticleBiomolecules & therapeutics2016

Anti-Proliferative and Pro-Apoptotic Activities of 4-Methyl-2,6-bis(1-phenylethyl)phenol in Cancer Cells.

Nak Yoon Sung, Seung Cheol Kim, Yun Hwan Kim, Gihyeon Kim, Yunmi Lee, Gi-Ho Sung, Ji Hye Kim, Woo Seok Yang, Mi Seon Kim, Kwang-Soo Baek and 2 more

Open access · greenAbstract read
In one paragraph

Article in Biomolecules & therapeutics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.4field-weighted citation impact, top 17% 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

6 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
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  6. Integrative cancer therapies
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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

12 authors at 4 institutions in 1 country.

Nak Yoon SungDepartment of Genetic Engineering, Sungkyunkwan University, Suwon 16419, Republic of Korea.
Seung Cheol KimDivision of Gynecologic Oncology Department of Obstetrics and Gynecology, Ewha Womans University Mokdong Hospital College of Medicine, Ewha Womans University, Seoul 03760, Republic of Korea.
Yun Hwan KimDivision of Gynecologic Oncology Department of Obstetrics and Gynecology, Ewha Womans University Mokdong Hospital College of Medicine, Ewha Womans University, Seoul 03760, Republic of Korea.
Gihyeon KimDepartment of Chemistry, Kwangwoon University, Seoul 01897, Republic of Korea.
Yunmi LeeDepartment of Chemistry, Kwangwoon University, Seoul 01897, Republic of Korea.
Gi-Ho SungInstitute for Bio-Medical Convergence, International St. Mary's Hospital and College of Medicine, Catholic Kwandong University, Incheon 22711, Republic of Korea.
Ji Hye KimDepartment of Genetic Engineering, Sungkyunkwan University, Suwon 16419, Republic of Korea.
Woo Seok YangDepartment of Genetic Engineering, Sungkyunkwan University, Suwon 16419, Republic of Korea.
Mi Seon KimDepartment of Genetic Engineering, Sungkyunkwan University, Suwon 16419, Republic of Korea.
Kwang-Soo BaekDepartment of Genetic Engineering, Sungkyunkwan University, Suwon 16419, Republic of Korea.
Jong-Hoon KimDepartment of Veterinary Physiology, College of Veterinary Medicine, Chonbuk National University, Iksan 54596, Republic of Korea.
Jae Youl ChoDepartment of Genetic Engineering, Sungkyunkwan University, Suwon 16419, Republic of Korea.
Sungkyunkwan University · KRCatholic Kwandong University International St. Mary's Hospital · KREwha Womans University · KRKwangwoon University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

It has been found that 4-isopropyl-2,6-bis(1-phenylethyl)phenol (KTH-13), a novel compound isolated from Cordyceps bassiana, is able to suppress tumor cell proliferation by inducing apoptosis. To mass-produce this compound, we established a total synthesis method. Using those conditions, we further synthesized various analogs with structural similarity to KTH-13. In this study, we aimed to test their anti-cancer activity by measuring anti-proliferative and pro-apoptotic activities. Of 8 compounds tested, 4-methyl-2,6-bis(1-phenylethyl)phenol (KTH-13-Me) exhibited the strongest anti-proliferative activity toward MDA-MB 231 cells. KTH-13-Me also similarly suppressed the survival of various cancer cell lines, including C6 glioma, HCT-15, and LoVo cells. Treatment of KTH-13-Me induced several apoptotic signs in C6 glioma cells, such as morphological changes, induction of apoptotic bodies, and nuclear fragmentation and chromatin condensation. Concordantly, early-apoptotic cells were also identified by staining with FITC-Annexin V/PI. Moreover, KTH-13-Me highly enhanced the activation of caspase-3 and caspase-9, and decreased the protein level of Bcl-2. In addition, the phosphorylation levels of Src and STAT3 were diminished in KTH-13-Me-treated C6 cells. Therefore, these results suggest that KTH-13-Me can be developed as a novel anti-cancer drug capable of blocking proliferation, inducing apoptosis, and blocking cell survival signaling in cancer cells.

Indexed as

4-methyl-26-bis(1-phenylethyl)phenolAnti-cancer activityApoptotisCordyceps Bassiana

Identifiers

PMID27068261
PMCPMC4930284
OpenAlexW2312959634

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.