Evidence map›Paper›PMID 28936721›Full record

ArticleMolecular and cellular biochemistry2018

A novel resveratrol derivative selectively inhibits the proliferation of colorectal cancer cells with KRAS mutation.

Haruna Okamoto, Taiji Matsukawa, Satoshi Doi, Toshiyuki Tsunoda, Yuuga Sawata, Madoka Naemura, Koichiro Ohnuki, Senji Shirasawa, Yojiro Kotake

Abstract read
PubMed Publisher
In one paragraph

Article in Molecular and cellular biochemistry, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.0field-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

2 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Cancer genomics & proteomics
    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

9 authors at 2 institutions in 1 country.

Haruna OkamotoGraduate School of Humanity-Oriented Science and Engineering, Kindai University, 11-6 Kayanomori, Iizuka, Fukuoka, 820-8555, Japan.
Taiji MatsukawaTechnology Development Section, UHA Mikakuto Co., Ltd, 4-12 Kanzaki-cho, Chuo-ku, Osaka, 540-0016, Japan.
Satoshi DoiTechnology Development Section, UHA Mikakuto Co., Ltd, 4-12 Kanzaki-cho, Chuo-ku, Osaka, 540-0016, Japan.
Toshiyuki TsunodaDepartment of Cell Biology, Faculty of Medicine, Fukuoka University, 7-45-1 Nanakuma, Jonan-ku, Fukuoka, 814-0180, Japan.
Yuuga SawataGraduate School of Humanity-Oriented Science and Engineering, Kindai University, 11-6 Kayanomori, Iizuka, Fukuoka, 820-8555, Japan.
Madoka NaemuraGraduate School of Humanity-Oriented Science and Engineering, Kindai University, 11-6 Kayanomori, Iizuka, Fukuoka, 820-8555, Japan.
Koichiro OhnukiGraduate School of Humanity-Oriented Science and Engineering, Kindai University, 11-6 Kayanomori, Iizuka, Fukuoka, 820-8555, Japan.
Senji ShirasawaDepartment of Cell Biology, Faculty of Medicine, Fukuoka University, 7-45-1 Nanakuma, Jonan-ku, Fukuoka, 814-0180, Japan.
Yojiro KotakeGraduate School of Humanity-Oriented Science and Engineering, Kindai University, 11-6 Kayanomori, Iizuka, Fukuoka, 820-8555, Japan. ykotake@fuk.kindai.ac.jp.
Kindai University · JPFukuoka University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Resveratrol is a polyphenolic compound in many edible foods including grapes, peanuts, and berries. Several studies have revealed the beneficial effects of resveratrol against various diseases such as heart disease, diabetes, obesity, neurological disorders, and cancer. A recent study showed that resveratrol inhibits the proliferation of HCT116 human colorectal cancer cells in three-dimensional culture (3DC) via induction of luminal apoptosis in HCT116 cell spheroids. In this study, we showed that a novel compound, caffeic acid-adducted resveratrol, has a stronger inhibitory effect on the growth of HCT116 cell spheroids in 3DC than resveratrol. It showed almost the same inhibitory efficacy as 5-fluorouracil, a conventional anticancer drug. We further showed that the resveratrol derivative did not affect the growth of HKe3 cell spheroids derived from HCT116 cells by disruption of the activating mutant KRAS gene. These results suggest that the resveratrol derivative inhibits the growth of HCT116 cell spheroids via inhibition of an oncogenic KRAS-mediated signaling pathway.

Indexed as

MutationCell ProliferationColorectal NeoplasmsHumansMCF-7 CellsProto-Oncogene Proteins p21(ras)ResveratrolSignal TransductionStilbenesKRAS protein, humanProto-Oncogene Proteins p21(ras)ResveratrolStilbenesColorectal cancerKRASOncogeneResveratrolThree-dimensional culture

Identifiers

PMID28936721
OpenAlexW2760394106

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.