Evidence map›Paper›PMID 32141266›Full record

ArticleJournal of biomedical optics2020

Diffuse reflectance spectroscopy to monitor murine colorectal tumor progression and therapeutic response.

Ariel I Mundo, Gage J Greening, Michael J Fahr, Lawrence N Hale, Elizabeth A Bullard, Narasimhan Rajaram, Timothy J Muldoon

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Journal of biomedical optics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.9field-weighted citation impact, top 21% 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

5 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Minimally invasiveMethodsX · 2022
    Article
  5. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 1 institution in 1 country.

Ariel I MundoUniversity of Arkansas, Department of Biomedical Engineering, Fayetteville, Arkansas, United States.
Gage J GreeningUniversity of Arkansas, Department of Biomedical Engineering, Fayetteville, Arkansas, United States.
Michael J FahrUniversity of Arkansas, Department of Computer Science, Fayetteville, Arkansas, United States.
Lawrence N HaleUniversity of Arkansas, Department of Chemistry and Biochemistry, Fayetteville, Arkansas, United States.
Elizabeth A BullardUniversity of Arkansas, Department of Biomedical Engineering, Fayetteville, Arkansas, United States.
Narasimhan RajaramUniversity of Arkansas, Department of Biomedical Engineering, Fayetteville, Arkansas, United States.
Timothy J MuldoonUniversity of Arkansas, Department of Biomedical Engineering, Fayetteville, Arkansas, United States.
University of Arkansas at Fayetteville · US

Funding

The role of optical biomarkers in endoscopic detection and therapeutic monitoring of gastrointestinal cancerR15CA202662 · NCI · UNIVERSITY OF ARKANSAS AT FAYETTEVILLE · PI MULDOON, TIMOTHY J · 2016 to 2016
$442k
NCI NIH HHS R15 CA202662
6 · The paper itself

Abstract

significanceMany studies in colorectal cancer (CRC) use murine ectopic tumor models to determine response to treatment. However, these models do not replicate the tumor microenvironment of CRC. Physiological information of treatment response derived via diffuse reflectance spectroscopy (DRS) from murine primary CRC tumors provide a better understanding for the development of new drugs and dosing strategies in CRC.

aimTumor response to chemotherapy in a primary CRC model was quantified via DRS to extract total hemoglobin content (tHb), oxygen saturation (StO2), oxyhemoglobin, and deoxyhemoglobin in tissue. APPROACH: A multimodal DRS and imaging probe (0.78 mm outside diameter) was designed and validated to acquire diffuse spectra longitudinally-via endoscopic guidance-in developing colon tumors under 5-fluoruracil (5-FU) maximum-tolerated (MTD) and metronomic regimens. A filtering algorithm was developed to compensate for positional uncertainty in DRS measurements Results: A maximum increase in StO2 was observed in both MTD and metronomic chemotherapy-treated murine primary CRC tumors at week 4 of neoadjuvant chemotherapy, with 21  ±  6  %   and 17  ±  6  %   fold changes, respectively. No significant changes were observed in tHb.

conclusionOur study demonstrates the feasibility of DRS to quantify response to treatment in primary CRC models.

Indexed as

Disease Models, AnimalAnimalsAntimetabolites, AntineoplasticBiomarkers, TumorColorectal NeoplasmsDisease ProgressionFemaleFluorouracilHemoglobinsMiceMice, Inbred AOptical ImagingOxygenPrecancerous ConditionsSpectrophotometryAntimetabolites, AntineoplasticBiomarkers, TumorFluorouracilHemoglobinsOxygenazoxymethanecolon cancerdiffuse reflectance spectroscopyendoscopyhemoglobin contentmetronomic chemotherapyneoadjuvant chemotherapyoxygen saturation

Identifiers

PMID32141266
PMCPMC7058691
OpenAlexW4249123263

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.