Evidence map›Paper›PMID 33660534›Full record

ArticleIntegrative cancer therapies

Resuming Sensitivity of Tamoxifen-Resistant Breast Cancer Cells to Tamoxifen by Tetrandrine.

Yuntao Wang, Wei Yue, Haiyan Lang, Xiaoqing Ding, Xinyi Chen, Haiyan Chen

Open access · goldAbstract read
In one paragraph

Article in Integrative cancer therapies. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.7field-weighted citation impact, top 11% 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

13 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. Dual role of autophagy in bone metastasis: mechanistic insights and therapeutic targeting.American journal of clinical and experimental urology · 2025
    Review
  3. Tetrandrine for Targeting Therapy Resistance in Cancer.Current topics in medicinal chemistry · 2024
    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

6 authors at 4 institutions in 2 countries.

Yuntao WangBeijing Yuyuan Dian of Xingzhitang TCM Clinic, Beijing, China.
Wei YueUniversity of Virginia Health System, Charlottesville, VA, USA.
Haiyan LangDongfang Hospital affiliated to Beijing University of Traditional Chinese Medicine, Beijing, China.
Xiaoqing DingDongfang Hospital affiliated to Beijing University of Traditional Chinese Medicine, Beijing, China.
Xinyi ChenDongzhimen Hospital affiliated to Beijing University of Traditional Chinese Medicine, Beijing, China.
Haiyan ChenDongfang Hospital affiliated to Beijing University of Traditional Chinese Medicine, Beijing, China.ORCID 0000-0002-5829-5783
Beijing Hospital of Traditional Chinese Medicine · CNDongzhimen Hospital Affiliated to Beijing University of Chinese Medicine · CNTang Hospital · CNUniversity of Virginia Health System · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTamoxifen is one of the medicines for adjuvant endocrine therapy of hormone-dependent breast cancer. However, development of resistance to tamoxifen occurs inevitably during treatment. This study aimed to determine whether sensitivity of tamoxifen-resistant breast cancer cells (TAM-R) could be reinstated by tetrandrine (Tet).

methodsAll experiments were conducted in TAM-R cells derived from the MCF-7 breast cancer cell line by long-term tamoxifen exposure. Cell growth, apoptosis, and autophagy were end-points that evaluated the effect of Tet (0.9 μg/ml, 1.8 μg/ml, and 3.75 μg/ml) alone or in combination with TAM (1 μM). Cell apoptosis was determined by an ELISA assay and autophagy was determined by fluorescent staining using the Enzo autophagy detection kit. Immunoblotting was used to evaluate markers for apoptosis, autophagy, and related signal pathway molecules.

resultsGrowth of TAM-R cells was significantly inhibited by Tet. Combination of Tet with tamoxifen induced a greater inhibition on cell growth than tamoxifen alone, which was predominantly due to enhancement of pro-apoptotic effect of TAM by Tet. Autophagy was significantly inhibited in TAM-R cells treated with Tet plus TAM as shown by increased autophagosomes and the levels of LC3-II and p62. At 0.9 μg/ml, Tet increased the levels of both apoptosis and autophagy markers. Among them increase in p53 levels was more dramatic.

conclusionsTet as a monotherapy inhibits TAM-R cells. Tet potentiates the pro-apoptotic effect of TAM via inhibition of autophagy.

Indexed as

BenzylisoquinolinesBreast NeoplasmsAntineoplastic Agents, HormonalApoptosisCell Line, TumorDrug Resistance, NeoplasmFemaleHumansMCF-7 CellsTamoxifenAntineoplastic Agents, HormonalBenzylisoquinolinesTamoxifentetrandrineapoptosisautophagytamoxifentamoxifen-resistant breast cancer cellstetrandrine

Identifiers

PMID33660534
PMCPMC8164553
OpenAlexW3135257864

What OpenQuestion holds

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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.