Evidence map›Paper›PMID 30634506›Full record

ArticleCancers2019

Paroxetine Induces Apoptosis of Human Breast Cancer MCF-7 Cells through Ca

Young-Woo Cho, Eun-Jin Kim, Marie Merci Nyiramana, Eui-Jung Shin, Hana Jin, Ji Hyeon Ryu, Kee Ryeon Kang, Gyeong-Won Lee, Hye Jung Kim, Jaehee Han and 1 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed, 1 pooled it
5.6field-weighted citation impact, top 4% 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

31 citing papers in PubMed, 1 synthesis or guideline pooled it, 65 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Drug Repositioning in Doxorubicin-Induced Cardiotoxicity Protection.International journal of molecular sciences · 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

11 authors at 1 institution in 1 country.

Young-Woo ChoDepartment of Physiology, College of Medicine and Institute of Health Sciences, Gyeongsang National University, Jinju 52727, Korea. ywcho@kbiohealth.kr.
Eun-Jin KimDepartment of Physiology, College of Medicine and Institute of Health Sciences, Gyeongsang National University, Jinju 52727, Korea. eunjin1981@hanmail.net.
Marie Merci NyiramanaDepartment of Physiology, College of Medicine and Institute of Health Sciences, Gyeongsang National University, Jinju 52727, Korea. mariemerci0222@gmail.com.
Eui-Jung ShinDepartment of Physiology, College of Medicine and Institute of Health Sciences, Gyeongsang National University, Jinju 52727, Korea. eui-jung@naver.com.
Hana JinDepartment of Pharmacology, College of Medicine and Institute of Health Sciences, Gyeongsang National University, Jinju 52727, Korea. hanajin.kr@daum.net.
Ji Hyeon RyuDepartment of Physiology, College of Medicine and Institute of Health Sciences, Gyeongsang National University, Jinju 52727, Korea. wlgus9217@naver.com.ORCID 0000-0003-0342-3108
Kee Ryeon KangDepartment of Biochemistry, College of Medicine and Institute of Health Sciences, Gyeongsang National University, Jinju 52727, Korea. kkang@gnu.ac.kr.
Gyeong-Won LeeDivision of Hematology-Oncology, Department of Internal Medicine, College of Medicine and Institute of Health Sciences, Gyeongsang National University, Jinju 52727, Korea. brightree24@gmail.com.ORCID 0000-0002-1781-2262
Hye Jung KimDepartment of Pharmacology, College of Medicine and Institute of Health Sciences, Gyeongsang National University, Jinju 52727, Korea. hyejungkim@gnu.ac.kr.ORCID 0000-0002-7067-6810
Jaehee HanDepartment of Physiology, College of Medicine and Institute of Health Sciences, Gyeongsang National University, Jinju 52727, Korea. jheehan@gnu.ac.kr.
Dawon KangDepartment of Physiology, College of Medicine and Institute of Health Sciences, Gyeongsang National University, Jinju 52727, Korea. dawon@gnu.ac.kr.ORCID 0000-0001-7402-7298
Gyeongsang National University · KR

Funding

Ministry of Education, Science and Technology NRF-2010-0024258Ministry of Science ICT and Future Planning NRF-2015R1A-5A2-008833
6 · The paper itself

Abstract

Depression is more common in women with breast cancer than the general population. Selective serotonin reuptake inhibitors (SSRIs), a group of antidepressants, are widely used for the treatment of patients with depression and a range of anxiety-related disorders. The association between the use of antidepressant medication and breast cancer is controversial. In this study, we investigated whether and how SSRIs induce the death of human breast cancer MCF-7 cells. Of the antidepressants tested in this study (amitriptyline, bupropion, fluoxetine, paroxetine, and tianeptine), paroxetine most reduced the viability of MCF-7 cells in a time-and dose-dependent manner. The exposure of MCF-7 cells to paroxetine resulted in mitochondrion-mediated apoptosis, which is assessed by increase in the number of cells with sub-G1 DNA content, caspase-8/9 activation, poly (ADP-ribose) polymerase cleavage, and Bax/Bcl-2 ratio and a reduction in the mitochondrial membrane potential. Paroxetine increased a generation of reactive oxygen species (ROS), intracellular Ca

Indexed as

apoptosisbreast cancercalciumdepressionMAPKparoxetinereactive oxygen species

Identifiers

PMID30634506
PMCPMC6356564
OpenAlexW2910297427

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.