Evidence map›Paper›PMID 28122339›Full record

ArticleOncotarget2017

Molecularly targeted co-delivery of a histone deacetylase inhibitor and paclitaxel by lipid-protein hybrid nanoparticles for synergistic combinational chemotherapy.

Hima Bindu Ruttala, Thiruganesh Ramasamy, Bijay Kumar Poudal, Yongjoo Choi, Ju Yeon Choi, Jeonghwan Kim, Sae Kwang Ku, Han-Gon Choi, Chul Soon Yong, Jong Oh Kim

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

18 citing papers in PubMed, 44 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Review
  6. Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Nanotechnology-Based Histone Deacetylase Inhibitors for Cancer Therapy.Frontiers in cell and developmental biology · 2020
    Review
  12. Article
  13. Review
  14. Review
  15. Article
  16. Article
  17. Article
  18. 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.

Hima Bindu RuttalaCollege of Pharmacy, Yeungnam University, Gyeongsan, 712-749, South Korea.
Thiruganesh RamasamyCollege of Pharmacy, Yeungnam University, Gyeongsan, 712-749, South Korea.
Bijay Kumar PoudalCollege of Pharmacy, Yeungnam University, Gyeongsan, 712-749, South Korea.
Yongjoo ChoiCollege of Pharmacy, Yeungnam University, Gyeongsan, 712-749, South Korea.
Ju Yeon ChoiCollege of Pharmacy, Yeungnam University, Gyeongsan, 712-749, South Korea.
Jeonghwan KimCollege of Pharmacy, Yeungnam University, Gyeongsan, 712-749, South Korea.
Sae Kwang KuCollege of Korean Medicine, Daegu Haany University, Gyeongsan, 712-715, South Korea.
Han-Gon ChoiCollege of Pharmacy, Institute of Pharmaceutical Science and Technology, Hanyang University, Sangnok-gu, Ansan 426-791, South Korea.
Chul Soon YongCollege of Pharmacy, Yeungnam University, Gyeongsan, 712-749, South Korea.
Jong Oh KimCollege of Pharmacy, Yeungnam University, Gyeongsan, 712-749, South Korea.
Yeungnam University · KRHanyang University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In this study, a transferrin-anchored albumin nanoplatform with PEGylated lipid bilayers (Tf-L-APVN) was developed for the targeted co-delivery of paclitaxel and vorinostat in solid tumors. Tf-L-APVN exhibited a sequential and controlled release profile of paclitaxel and vorinostat, with an accelerated release pattern at acidic pH. At cellular levels, Tf-L-APVN significantly enhanced the synergistic effects of paclitaxel and vorinostat on the proliferation of MCF-7, MDA-MB-231, and HepG2 cancer cells. Vorinostat could significantly enhance the cytotoxic potential of paclitaxel, induce marked cell apoptosis, alter cell cycle patterns, and inhibit the migratory capacity of cancer cells. In addition, Tf-L-APVN showed prolonged circulation in the blood and maintained an effective ratio of 1:1 (for paclitaxel and vorinostat) throughout the study period. In HepG2 tumor-bearing mice, Tf-L-APVN displayed excellent antitumor efficacy and the combination of paclitaxel and vorinostat significantly inhibited the tumor growth. Taken together, dual drug-loaded Tf receptor-targeted nanomedicine holds great potential in chemotherapy of solid tumors.

Indexed as

Adenoma, Liver CellAnimalsAntineoplastic Agents, PhytogenicApoptosisCell ProliferationDrug SynergismDrug Therapy, CombinationHistone Deacetylase InhibitorsHumansHydroxamic AcidsLipidsLiver NeoplasmsMaleMiceMice, Inbred BALB CMolecular Targeted TherapyAntineoplastic Agents, PhytogenicHistone Deacetylase InhibitorsHydroxamic AcidsLipidsPaclitaxelVorinostatalbuminhistone deacetylase inhibitorlipid bilayerpaclitaxeltransferrin

Identifiers

PMID28122339
PMCPMC5362455
OpenAlexW2578126608

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.