Evidence map›Paper›PMID 34466099›Full record

ArticleSaudi journal of biological sciences2021

Recombinant human Erythropoietin enhanced the cytotoxic effects of tamoxifen toward the spheroid MCF-7 breast cancer cells.

Hareth Y Shujaa Edin, Nagi A Al-Haj, Abdullah Rasedee, Noorjahan Banu Alitheen, Arifah Abdul Kadir, Chee Wun How, Heshu Sulaiman Rahman, Hussah Abdullah Al-Shwyeh

Abstract read
In one paragraph

Article in Saudi journal of biological sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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.

Hareth Y Shujaa EdinInstitute of Bioscience, Universiti Putra Malaysia,Malaysia.
Nagi A Al-HajFaculty of Medicine and Health Sciences, Sana'a University, Yemen.
Abdullah RasedeeFaculty of Veterinary Medicine, Universiti Putra Malaysia, Malaysia.
Noorjahan Banu AlitheenFaculty of Biotechnology and Biomolecular Sciences, University Putra Malaysia, Malaysia.
Arifah Abdul KadirFaculty of Veterinary Medicine, Universiti Putra Malaysia, Malaysia.
Chee Wun HowSchool of Pharmacy, Monash University Malaysia, Bandar Sunway, Selangor, Malaysia.
Heshu Sulaiman RahmanCollege of Medicine, University of Sulaimani, Kurdistan Region, Iraq.
Hussah Abdullah Al-ShwyehDepartment of Biology, College of Science, Imam Abdulrahman Bin Faisal University (IAU), Dammam 31441-1982, Saudi Arabia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Erythropoietin (EPO) is widely used to treat anemia in patients undergoing chemotherapy for cancers. The main objective of this study was to investigate the effect of rHuEPO on the response of spheroid breast cancer, MCF-7, cells to tamoxifen treatment. The MCF-7 spheroids were treated with 10 mg/mL tamoxifen in combination with either 0, 10, 100 or 200 IU/mL rHuEPO for 24, 48 or 72 h. The viability of the MCF-7 cells was determined using the annexin-V, cell cycle, caspases activation and acridine orange/propidium iodide staining. rHuEPO-tamoxifen combination significantly (p greater than 0.05) increased the number of spheroid MCF-7 cells entering early apoptotic phase after 12 h and late apoptotic phase after 24 h of treatment; primarily the result of the antiproliferative effect tamoxifen. Tamoxifen alone significantly (p < 0.05) increased the caspase-3 and -9 activities in the spheroid MCF-7 cells by 200 to 550% of the control. Combination rHuEPO and tamoxifen produced much lesser effect on the caspase-8 activity. The rHuEPO in the combination treatment had concentration-dependently caused decrease in the caspase activities. rHuEPO-tamoxifen combination markedly increased MCF-7 cells entering the SubG0/G1 phase of the cell cycle by more than 500% of the control, while decreasing those entering the G2 + M and S phases by 50%. After 72 h, the combination treatment produced greater (p < 0.05) change in the SubG0/G1 phase than tamoxifen treatment alone. Morphologically, spheroid MCF-7 cells subjected to combination rHuEPO-tamoxifen treatment showed nuclear condensation and margination, cytoplasmic blebbing, necrosis, and early and late apoptosis. Thus, the study showed that rHuEPO-tamoxifen combination induced apoptosis in the spheroid MCF-7 cells. The apoptotic effect of the rHuEPO-tamoxifen combination treatment on the MCF-7 cells was greater than that produced by tamoxifen alone. The rHuEPO-tamoxifen treatment enhanced the caspase-independent apoptotic effects of tamoxifen on the spheroid MCF-7 cells.

Indexed as

CC, correlation coefficientCV, coefficient of varianceDG, geometrical mean of diameterECRB, Eppendorf A-4-62 centrifuge rotor 1 MTP bucketsESBR, The Eppendorf swing-bucket rotor with tubes rackHanging dropHD, Hanging dropMCF-7, GMD, geometrical mean diameterMCF-7, human breast cell lineOLT, Overlay techniqueOverlay techniquepoly-HEMA, Poly 2-hydroxyethyl methacrylateRecombinant human erythropoietinrHuEPO, Recombinant human erythropoietinSpheroidsS, surface areaTamoxifenTAM Tamoxifen ULAT, ultra-low adhesive plateUltra-low adhesive plate

Identifiers

PMID34466099
PMCPMC8381065

What OpenQuestion holds

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LicenceCC BY-NC-ND
Read underepoch 390

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.