Evidence map›Paper›PMID 38148070›Full record

ArticleIn vivo (Athens, Greece)

Polyphyllin II (PPII) Enhances the Sensitivity of Multidrug-resistant A549/DDP Cells to Cisplatin by Modulating Mitochondrial Energy Metabolism.

Lian Peng, Renyi Yang, Zhibing Wang, Huiying Jian, Xiaoning Tan, Jian Li, Zuomei He, Rui Huang, Puhua Zeng, Wenhui Gao

Open access · diamondAbstract read
In one paragraph

Article in In vivo (Athens, Greece). The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.7field-weighted citation impact, top 15% 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

6 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. NLRP1 inhibits lung adenocarcinoma growth through mediating mitochondrial dysregulation in an inflammasome-independent manner.Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica · 2024
    Article
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

10 authors at 3 institutions in 1 country.

Lian PengHunan University of Chinese Medicine, Changsha, Hunan, P.R. China.
Renyi YangHunan University of Chinese Medicine, Changsha, Hunan, P.R. China.
Zhibing WangHunan University of Chinese Medicine, Changsha, Hunan, P.R. China.
Huiying JianKey Laboratory of TCM Formula and Syndrome Transformation Medicine, Changsha, Hunan, P.R. China.
Xiaoning TanHunan University of Chinese Medicine, Changsha, Hunan, P.R. China.
Jian LiKey Laboratory of TCM Formula and Syndrome Transformation Medicine, Changsha, Hunan, P.R. China.
Zuomei HeCancer Research Institute of Hunan Academy of Traditional Chinese Medicine, Changsha, Hunan, P.R. China.
Rui HuangCancer Research Institute of Hunan Academy of Traditional Chinese Medicine, Changsha, Hunan, P.R. China.
Puhua ZengKey Laboratory of TCM Formula and Syndrome Transformation Medicine, Changsha, Hunan, P.R. China; zph120@126.com.
Wenhui GaoHunan University of Chinese Medicine, Changsha, Hunan, P.R. China; 476541034@qq.com.
Hunan Academy of Traditional Chinese Medicine · CNHunan University of Traditional Chinese Medicine · CNHunan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND/

aimCisplatin resistance often leads to treatment futility and elevated mortality rates in patients with lung cancer. One promising strategy to address this challenge involves the integration of traditional Chinese medicine (TCM) with chemotherapeutic drugs. Currently, the potential synergistic effect and underlying mechanism of polyphyllin II (PPII) and cisplatin combination in combating cisplatin (DDP) resistance in lung cancer remain unexplored. MATERIALS AND

methodsIn this study, we established a cisplatin resistance model using A549 cells and explored the underlying mechanisms of PPII in combination with cisplatin in A549/DDP resistant cells. Specifically, we assessed the impact of PPII combined with cisplatin on A549/DDP cell proliferation, viability, and the expression of apoptosis-related proteins. To gain deeper insights into the underlying mechanism, we examined the effects of PPII and cisplatin on mitochondrial function in A549/DDP cells.

resultsThis combination induced cell cycle arrest at both the S phase and G

conclusionThe combination of PPII and cisplatin effectively modulated the mitochondrial function, thereby reversing drug resistance in A549/DDP cells. This innovative combination therapy shows significant promise as a novel strategy for overcoming cisplatin resistance in lung cancer.

Indexed as

Antineoplastic AgentsLung NeoplasmsA549 CellsApoptosisApoptosis Regulatory ProteinsCell Line, TumorCell ProliferationCisplatinDrug Resistance, NeoplasmEnergy MetabolismHumansMitochondriaSaponinsSteroidsAntineoplastic AgentsApoptosis Regulatory ProteinsCisplatinpolyphyllin IISaponinsSteroidsapoptosiscisplatinLung cancermitochondriaPPII

Identifiers

PMID38148070
PMCPMC10756451
OpenAlexW4390236425

What OpenQuestion holds

Textmetadata
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.