Evidence map›Paper›PMID 29191192›Full record

ArticleBMC complementary and alternative medicine2017

Anticancer activities of ethanol extract from the Antarctic freshwater microalga, Botryidiopsidaceae sp.

Sung-Suk Suh, Sun-Mi Kim, Jung Eun Kim, Ju-Mi Hong, Sung Gu Lee, Ui Joung Youn, Se Jong Han, Il-Chan Kim, Sanghee Kim

Abstract read
In one paragraph

Article in BMC complementary and alternative medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
–field-weighted citation impact
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

10 citing papers in PubMed.

  1. Article
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  5. Ecological interactions in glacier environments: a review of studies on a model Alpine glacier.Biological reviews of the Cambridge Philosophical Society · 2025
    Review
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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

9 authors.

Sung-Suk SuhDivision of Polar Life Sciences, Korea Polar Research Institute, Incheon, 21990, Republic of Korea.
Sun-Mi KimDivision of Polar Life Sciences, Korea Polar Research Institute, Incheon, 21990, Republic of Korea.
Jung Eun KimDivision of Polar Life Sciences, Korea Polar Research Institute, Incheon, 21990, Republic of Korea.
Ju-Mi HongDivision of Polar Life Sciences, Korea Polar Research Institute, Incheon, 21990, Republic of Korea.
Sung Gu LeeDivision of Polar Life Sciences, Korea Polar Research Institute, Incheon, 21990, Republic of Korea.
Ui Joung YounDivision of Polar Life Sciences, Korea Polar Research Institute, Incheon, 21990, Republic of Korea.
Se Jong HanDivision of Polar Life Sciences, Korea Polar Research Institute, Incheon, 21990, Republic of Korea.
Il-Chan KimDivision of Polar Life Sciences, Korea Polar Research Institute, Incheon, 21990, Republic of Korea. ickim@kopri.re.kr.
Sanghee KimDivision of Polar Life Sciences, Korea Polar Research Institute, Incheon, 21990, Republic of Korea. sangheekim@kopri.re.kr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCancer is a leading cause of human death around the world and occurs through the highly complex coordination of multiple cellular pathways. Recent studies have revealed that microalgal extracts exhibit considerable pharmaceutical activities, including those against various cancer cells. Thus, microalgae are promising candidates as novel cancer therapeutic drugs. In this study, we evaluated the biological functions of the ethanolic extract of the Antarctic freshwater microalga, Bo tryidiopsidaceae sp., such as its antioxidant, anti-proliferative, apoptotic and anti-invasive properties.

methodsTo estimate antioxidant capacity of ethanol extract of Bo tryidiopsidaceae sp. (ETBO), free radical 2,2'-azino-bis (3-ethylbenzthiazoline-6-sulphonic acid) (ABTS) and 1,1-diphenyl-2-picrylhydrazyl (DPPH) assays were used. The anti-proliferative activity of ETBO was assessed in several cancer cell lines (A375, Hs578T and HeLa) and non-tumorigenic keratinocyte cells (HaCaT), using MTT assay. In addition, Annexin V binding was performed to detect ETBO-induced apoptotic cells, and the expression levels of apoptosis-regulating proteins, caspase-3, p53, and Bcl-2, were determined by western blot. Boyden chamber assays were used to determine anti-migratory and anti-invasive properties of ETBO.

resultsETBO exhibited antioxidant activity and concentration-dependent anticancer activities, such as anti-proliferation and pro-apoptotic activities against cancer cells. Furthermore, the expression of the apoptosis-inducing proteins, p53 and caspase-3, significantly increased in response to ETBO, whereas the expression of the anti-apoptotic protein, Bcl-2, decreased. These data imply that ETBO induces apoptosis by caspase activation through the modulation of pro-apoptotic and anti-apoptotic gene, p53 and Bcl-2, respectively. In addition, ETBO significantly inhibited migration and invasion of cervical cancer cells in a concentration-dependent manner.

conclusionIn this study, ETBO exhibited considerable anticancer activities, such as inhibition of proliferation, invasion, and migration, as well as induction of apoptosis. These data suggest that ETBO is a promising therapeutic agent in cancer therapy and drug discovery.

Indexed as

Antarctic RegionsAntineoplastic AgentsApoptosisCell Line, TumorCell MovementCell ProliferationFresh WaterHeLa CellsHumansMicroalgaePlant ExtractsStramenopilesAntineoplastic AgentsPlant ExtractsAntarctic freshwater microalgaAnticancer activitiesAnti-proliferationBotryidiopsidaceae sp.

Identifiers

PMID29191192
PMCPMC5709829

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Registered trials

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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.