Evidence map›Paper›PMID 34599546›Full record

ArticleCell proliferation2021

Aptamer-conjugated mesoporous polydopamine for docetaxel targeted delivery and synergistic photothermal therapy of prostate cancer.

Liang Dai, Dapeng Wei, Jidong Zhang, Tianyu Shen, Yuming Zhao, Junqiang Liang, Wangteng Ma, Limin Zhang, Qingli Liu, Yue Zheng

Open access · goldAbstract read
In one paragraph

Article in Cell proliferation, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

19 citing papers in PubMed, 44 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. Article
  10. Review
  11. Article
  12. Review
  13. Article
  14. Review
  15. Review
  16. Article
  17. Review
  18. Review
  19. 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 2 institutions in 1 country.

Liang DaiDepartment of Urology, The First Hospital of Qinhuangdao, Qinhuangdao, China.
Dapeng WeiDepartment of Urology, The First Hospital of Qinhuangdao, Qinhuangdao, China.
Jidong ZhangDepartment of Urology, The First Hospital of Qinhuangdao, Qinhuangdao, China.
Tianyu ShenState Key Laboratory of Medicinal Chemical Biology, School of Medicine, Nankai University, Tianjin, China.
Yuming ZhaoDepartment of Urology, The First Hospital of Qinhuangdao, Qinhuangdao, China.
Junqiang LiangDepartment of Urology, The First Hospital of Qinhuangdao, Qinhuangdao, China.
Wangteng MaDepartment of Urology, The First Hospital of Qinhuangdao, Qinhuangdao, China.
Limin ZhangDepartment of Urology, The First Hospital of Qinhuangdao, Qinhuangdao, China.
Qingli LiuDepartment of Urology, The First Hospital of Qinhuangdao, Qinhuangdao, China.
Yue ZhengDepartment of Gastroenterology, The First Hospital of Qinhuangdao, Qinhuangdao, China.ORCID https://orcid.org/0000-0001-5844-5924
First Hospital of Qinhuangdao · CNNankai University · CN

Funding

Qinhuangdao Science and Technology Research and Development Foundation 201602A110Qinhuangdao Science and Technology Research and Development Foundation 201902A216Qinhuangdao Science and Technology Research and Development Foundation 202004A041
6 · The paper itself

Abstract

objectivesIt is imperative to develop efficient strategies on the treatment of prostate cancer. Here, we constructed multifunctional nanoparticles, namely AS1411@MPDA-DTX (AMD) for targeted and synergistic chemotherapy/photothermal therapy of prostate cancer. MATERIALS AND

methodsMesoporous polydopamine (MPDA) nanoparticles were prepared by a one-pot synthesis method, DTX was loaded through incubation, and AS1411 aptamer was modified onto MPDA by the covalent reaction. The prepared nanoparticles were characterized by ultra-micro spectrophotometer, Fourier transform infrared spectra, transmission electron microscope, and so on. The targeting ability was detected by selective uptake and cell killing. The mechanism of AMD-mediated synergistic therapy was detected by Western blot and immunofluorescence.

resultsThe prepared nanoparticles can be easily synthesized and possessed excellent water solubility, stability, and controlled drug release ability, preferentially in acidic context. Based on in vitro and in vivo results, the nanoparticles can efficiently target prostate cancer cells, promote DTX internalization, and enhance the antitumor effects of chemo-photothermal therapy strategies under the NIR laser irradiation.

conclusionsAs a multifunctional nanoplatform, AS1411@MPDA-DTX could efficiently target prostate cancer cells, promote DTX internalization, and synergistically enhance the antiprostate cancer efficiency by combining with NIR irradiation.

Indexed as

Cell Line, TumorDocetaxelDoxorubicinDrug Delivery SystemsHumansIndolesMaleNanoparticlesPhotothermal TherapyPolymersPorosityProstatic NeoplasmsDocetaxelDoxorubicinIndolespolydopaminePolymersaptamerchemo-photothermal therapydocetaxelmesoporous polydopamineprostate cancer

Identifiers

PMID34599546
PMCPMC8560597
OpenAlexW3203019544

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.