Evidence map›Paper›PMID 36926453›Full record

ArticleACS pharmacology & translational science2023

Rational Drug Design of Targeted and Enzyme-Cleavable Vitamin E Analogs as a Neoadjuvant to Chemotherapy:

Raghu S Pandurangi, Orsolya Cseh, Hema Artee Luchman, Cynthia Xiuguang Ma, Sanjeewa N Senadheera, Marcus Laird Forrest

Open access · greenAbstract read
In one paragraph

Article in ACS pharmacology & translational science, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.9field-weighted citation impact, top 26% 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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
  2. Article
  3. Frontiers in oncology · 2023
    Article
  4. Targeted Sensitization of Glioblastoma Multiforme Using AAAPT Technology.IEEE open journal of engineering in medicine and biology · 2023
    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

6 authors at 2 institutions in 1 country.

Raghu S PandurangiSci-Engi-Medco Solutions Inc. (SEMCO), 573, Lexington Landing Pl, St. Charles, Missouri 63303, United States.ORCID https://orcid.org/0000-0002-8143-2627
Orsolya CsehHRIC 2A25, 3330 Hospital Drive NW, Calgary, AB T2N 4N, Canada.
Hema Artee LuchmanHRIC 2A25, 3330 Hospital Drive NW, Calgary, AB T2N 4N, Canada.
Cynthia Xiuguang MaSiteman Cancer Center, Washington University School of Medicine, St. Louis, Missouri 63110, United States.
Sanjeewa N SenadheeraDepartment of Pharmaceutical Chemistry, School of Pharmacy, University of Kansas, Lawrence, Kansas 66047, United States.
Marcus Laird ForrestDepartment of Pharmaceutical Chemistry, School of Pharmacy, University of Kansas, Lawrence, Kansas 66047, United States.ORCID https://orcid.org/0000-0002-0288-6138
University of Kansas · USWashington University in St. Louis · US

Funding

Theranostics of Reduction of Cardiotoxicity Using Targeted Apoptosis Activation TechnologyR43CA214223 · NCI · SCI-ENGI-MEDCO SOLUTIONS, INC. · PI GABRIELSON, KATHLEEN LOUISE, PANDURANGI, RAGHU S · 2017 to 2017
$274k
NCI NIH HHS R43 CA214223
6 · The paper itself

Abstract

Traditional drug design focuses on specific biological targets where specific receptors or biomarkers are overexpressed by cancer cells. Cancer cells circumvent the interventions by activating survival pathways and/or downregulating cell death pathways for their survival. A priori activation of apoptosis pathways of tumor (AAAPT) is a novel tumor-sensitizing technology that sensitizes tumor cells that are not responding well to the current treatments by targeting specific survival pathways involved in the desensitization of tumor cells and tries to revive them selectively in cancer cells, sparing normal cells. Several vitamin E derivatives (AMP-001, AMP-002, AMP-003, and AMP-004) were synthesized, characterized, and studied for their anti-tumorigenic properties and their synergistic potential with the standard chemotherapy doxorubicin in various cancer cells including brain cancer stem cells

Identifiers

PMID36926453
PMCPMC10012254
OpenAlexW4319303489

What Socratic 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 Socratic graph.