Evidence map›Paper›PMID 27231935›Full record

ArticleNutrients2016

Cuminaldehyde from Cinnamomum verum Induces Cell Death through Targeting Topoisomerase 1 and 2 in Human Colorectal Adenocarcinoma COLO 205 Cells.

Kuen-Daw Tsai, Yi-Heng Liu, Ta-Wei Chen, Shu-Mei Yang, Ho-Yiu Wong, Jonathan Cherng, Kuo-Shen Chou, Jaw-Ming Cherng

Open access · goldAbstract read
In one paragraph

Article in Nutrients, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

14 citing papers in PubMed, 46 citations in OpenAlex.

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    Article
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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

8 authors at 4 institutions in 2 countries.

Kuen-Daw TsaiDepartment of Internal Medicine, China Medical University Beigang Hospital, Yunlin 65152, Taiwan. d4295@yahoo.com.tw.
Yi-Heng LiuDepartment of Internal Medicine, China Medical University Beigang Hospital, Yunlin 65152, Taiwan. yeeheng6061@gmail.com.
Ta-Wei ChenDepartment of Internal Medicine, China Medical University Beigang Hospital, Yunlin 65152, Taiwan. slowfish1234@yahoo.com.tw.
Shu-Mei YangDepartment of Internal Medicine, China Medical University Beigang Hospital, Yunlin 65152, Taiwan. kd2624@yahoo.com.tw.
Ho-Yiu WongDepartment of Internal Medicine, China Medical University Beigang Hospital, Yunlin 65152, Taiwan. pk1977wong@gmail.com.
Jonathan CherngFaculty of Medicine, Medical University of Lublin, Lublin 20-059, Poland. jcherngca@yahoo.com.tw.
Kuo-Shen ChouDepartment of Family Medicine, Saint Mary's Hospital Luodong, Yilan 26546, Taiwan. smh01062@smh.org.tw.
Jaw-Ming CherngDepartment of Internal Medicine, Saint Mary's Hospital Luodong, Yilan 26546, Taiwan. happy.professor@yahoo.com.
China Medical University · TWMedical University of Lublin · PLNational Chung Cheng University · TWSaint Mary's Hospital Luodong · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cinnamomum verum, also called true cinnamon tree, is employed to make the seasoning cinnamon. Furthermore, the plant has been used as a traditional Chinese herbal medication. We explored the anticancer effect of cuminaldehyde, an ingredient of the cortex of the plant, as well as the molecular biomarkers associated with carcinogenesis in human colorectal adenocarcinoma COLO 205 cells. The results show that cuminaldehyde suppressed growth and induced apoptosis, as proved by depletion of the mitochondrial membrane potential, activation of both caspase-3 and -9, and morphological features of apoptosis. Moreover, cuminaldehyde also led to lysosomal vacuolation with an upregulated volume of acidic compartment and cytotoxicity, together with inhibitions of both topoisomerase I and II activities. Additional study shows that the anticancer activity of cuminaldehyde was observed in the model of nude mice. Our results suggest that the anticancer activity of cuminaldehyde in vitro involved the suppression of cell proliferative markers, topoisomerase I as well as II, together with increase of pro-apoptotic molecules, associated with upregulated lysosomal vacuolation. On the other hand, in vivo, cuminaldehyde diminished the tumor burden that would have a significant clinical impact. Furthermore, similar effects were observed in other tested cell lines. In short, our data suggest that cuminaldehyde could be a drug for chemopreventive or anticancer therapy.

Indexed as

Cinnamomum zeylanicumAdenocarcinomaAnimalsAntineoplastic Agents, PhytogenicApoptosisBenzaldehydesCaspase 3Caspase 9Cell DeathCell Line, TumorCell ProliferationColorectal NeoplasmsCymenesDNA Topoisomerases, Type IDNA Topoisomerases, Type IIDose-Response Relationship, DrugAntineoplastic Agents, PhytogenicBenzaldehydesCASP3 protein, humanCASP9 protein, humanCaspase 3Caspase 9cuminaldehydeCymenesDNA Topoisomerases, Type IDNA Topoisomerases, Type IIPlant ExtractsTOP1 protein, humanTopoisomerase II InhibitorsTopoisomerase I Inhibitorsantiproliferativecuminaldehydelysosomal vacuolationtopoisomerase Itopoisomerase IIxenograft

Identifiers

PMID27231935
PMCPMC4924159
OpenAlexW2395695426

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.