Evidence map›Paper›PMID 29423106›Full record

ArticleOncotarget2018

The vascular disrupting agent combretastatin A-4 phosphate causes prolonged elevation of proteins involved in heme flux and function in resistant tumor cells.

Sanchareeka Dey, Sharda Kumari, Sarada Preeta Kalainayakan, James Campbell, Poorva Ghosh, Heling Zhou, Keely E FitzGerald, Maoping Li, Ralph P Mason, Li Zhang and 1 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

20 citing papers in PubMed, 42 citations in OpenAlex.

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  14. Longitudinal Photoacoustic Imaging of the Pharmacodynamic Effect of Vascular Targeted Therapy on Tumors.Clinical cancer research : an official journal of the American Association for Cancer Research · 2019
    Article
  15. Article
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  18. Article
  19. Review
  20. Osteopontin-targeted probe detects orthotopic breast cancers using optoacoustic imaging.Biotechnic & histochemistry : official publication of the Biological Stain Commission · 2018
    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

11 authors at 3 institutions in 2 countries.

Sanchareeka DeyDepartment of Biological Sciences, The University of Texas at Dallas, Richardson, TX, USA.
Sharda KumariDepartment of Radiology, The University of Texas Southwestern Medical Center, Dallas, TX, USA.
Sarada Preeta KalainayakanDepartment of Biological Sciences, The University of Texas at Dallas, Richardson, TX, USA.
James CampbellDepartment of Radiology, The University of Texas Southwestern Medical Center, Dallas, TX, USA.
Poorva GhoshDepartment of Biological Sciences, The University of Texas at Dallas, Richardson, TX, USA.
Heling ZhouDepartment of Radiology, The University of Texas Southwestern Medical Center, Dallas, TX, USA.
Keely E FitzGeraldDepartment of Biological Sciences, The University of Texas at Dallas, Richardson, TX, USA.
Maoping LiDepartment of Radiology, The University of Texas Southwestern Medical Center, Dallas, TX, USA.
Ralph P MasonDepartment of Radiology, The University of Texas Southwestern Medical Center, Dallas, TX, USA.
Li ZhangDepartment of Biological Sciences, The University of Texas at Dallas, Richardson, TX, USA.
Li LiuDepartment of Radiology, The University of Texas Southwestern Medical Center, Dallas, TX, USA.
The University of Texas at Dallas · USThe University of Texas Southwestern Medical Center · USChongqing Medical University · CN

Funding

UT Southwestern Medical Center Simmons Comprehensive Cancer CenterP30CA142543 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI Sandi Leigh Pruitt · 2010 to 2026
$53.7M
Optoacoustic Tomography System for Small AnimalsS10OD018094 · OD · UT SOUTHWESTERN MEDICAL CENTER · PI MASON, RALPH P. · 2015 to 2015
$510k
Small Animal Bioluminescence and Fluorescence Imaging System (with 3D capability)S10RR024757 · NCRR · UT SOUTHWESTERN MEDICAL CENTER · PI MASON, RALPH P. · 2007 to 2007
$335k
NCI NIH HHS P30 CA142543NCRR NIH HHS S10 RR024757NIH HHS S10 OD018094
6 · The paper itself

Abstract

Vascular disrupting agents (VDAs) represent a promising class of anti-cancer drugs for solid tumor treatment. Here, we aim to better understand the mechanisms underlying tumor reccurrence and treatment resistance following the administration of a VDA, combretastatin A-4 phosphate (CA4P). Firstly, we used photoacoustic tomography to noninvasively map the effect of CA4P on blood oxygen levels throughout subcutaneous non-small cell lung cancer (NSCLC) tumors in mice. We found that the oxygenation of peripheral tumor vessels was significantly decreased at 1 and 3 hours post-CA4P treatment. The oxygenation of the tumor core reduced significantly at 1 and 3 hours, and reached anoxia after 24 hours. Secondly, we examined the effect of CA4P on the levels of proteins involved in heme flux and function, which are elevated in lung tumors. Using immunohistochemistry, we found that CA4P substantially enhanced the levels of enzymes involved in heme biosynthesis, uptake, and degradation, as well as oxygen-utilizing hemoproteins. Furthermore, measurements of markers of mitochondrial function suggest that CA4P did not diminish mitochondrial function in resistant tumor cells. These results suggest that elevated levels of heme flux and function contribute to tumor regrowth and treatment resistance post-VDA administration.

Indexed as

combretastatin A-4 phosphate (CA4P)hemelung tumormultispectral optoacoustic tomography (MSOT)vascular disrupting agent (VDA)

Identifiers

PMID29423106
PMCPMC5790523
OpenAlexW2777959709

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.