Evidence map›Paper›PMID 30725348›Full record

ArticleMolecular biology reports2019

The anti-cancer effect of amygdalin on human cancer cell lines.

Asghar Arshi, Sayed Mostafa Hosseini, Fataneh Saleh Khaje Hosseini, Zahra Yousefnejad Amiri, Fatemeh Sadat Hosseini, Mahsa Sheikholia Lavasani, Hossein Kerdarian, Maryam Safarpour Dehkordi

Abstract read
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In one paragraph

Article in Molecular biology reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
2.0field-weighted citation impact, top 12% 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

8 citing papers in PubMed, 22 citations in OpenAlex.

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  6. Mineral Content and Volatile Profiling ofFoods (Basel, Switzerland) · 2022
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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 3 institutions in 1 country.

Asghar ArshiHuman Genetic Research Center, Baqiyatallah University of Medical Science, Tehran, Iran.ORCID http://orcid.org/0000-0002-8634-1089
Sayed Mostafa HosseiniHuman Genetic Research Center, Baqiyatallah University of Medical Science, Tehran, Iran. smhosseini@bmsu.ac.ir.ORCID http://orcid.org/0000-0003-3716-8133
Fataneh Saleh Khaje HosseiniDepartment of Biology, Science and Research Branch, Islamic Azad University, Tehran, Iran.ORCID http://orcid.org/0000-0002-4108-8630
Zahra Yousefnejad AmiriHuman Genetic Research Center, Baqiyatallah University of Medical Science, Tehran, Iran.ORCID http://orcid.org/0000-0002-3267-999X
Fatemeh Sadat HosseiniHuman Genetic Research Center, Baqiyatallah University of Medical Science, Tehran, Iran.ORCID http://orcid.org/0000-0003-4010-5547
Mahsa Sheikholia LavasaniHuman Genetic Research Center, Baqiyatallah University of Medical Science, Tehran, Iran.
Hossein KerdarianStudents Research Committee, Babol University of Medical Science, Babol, Iran.ORCID http://orcid.org/0000-0002-1837-9763
Maryam Safarpour DehkordiYoung Researchers and Elite Club, Shahrekord Branch, Islamic Azad University, Shahrekord, Iran.ORCID http://orcid.org/0000-0003-0482-0957
Baqiyatallah University of Medical Sciences · IRBabol University of Medical Sciences · IRIslamic Azad University of Shahrekord · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Derived from rosaceous plant seed, amygdalin belongs to aromatic cyanogenic glycoside group, and its anticancer effects have been supported by mounting evidence. In this study, we objected to investigate amygdalin effect on two antiapoptotic genes (Survivin, XIAP) and two lncRNAs (GAS5, MALAT1) in human cancer cells (A549, MCF7, AGS). Employing RT-qPCR analysis, we compared the mRNA levels of the genes related to apoptosis in A549, MCF7, and AGS cancer cells between amygdalin-treated (24, 48 and 72 h) and un-treated groups. RNA was extracted from both cell groups and then cDNAs were synthesized. The changes in the gene expression levels were specified using ΔΔCt method. RT-qPCR analysis has revealed that the expression of Survivin, XIAP, GAS5 and MALAT1 in amygdala-treated cancer cells were significantly different, compared to the un-treated cells. However, these expressions were different depending on the treatment time. According to the results, amygdalin significantly inhibited the expression level of Survivin, and XIAP genes in treated via untreated group. Our findings suggest that amygdalin might have an anticancer effect due to the various gene expressions in A549, MCF7, and AGS human cancer cells, showing it's potential as a natural therapeutic anticancer drug.

Indexed as

A549 CellsAmygdalinAntineoplastic AgentsApoptosisCell Line, TumorGene ExpressionHumansMCF-7 CellsRNA, Long NoncodingRNA, MessengerRNA, Small NucleolarSurvivinX-Linked Inhibitor of Apoptosis ProteinAmygdalinAntineoplastic Agentsgrowth arrest specific transcript 5MALAT1 long non-coding RNA, humanRNA, Long NoncodingRNA, MessengerRNA, Small NucleolarSurvivinXIAP protein, humanX-Linked Inhibitor of Apoptosis ProteinAmygdalinAntiapoptotic genesCancer cell lineLncRNAs

Identifiers

PMID30725348
OpenAlexW2914763271

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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.