Evidence map›Paper›PMID 39619119›Full record

ArticlePlastic and reconstructive surgery. Global open2024

A Novel Rat Model to Simulate Positive Margins in the Wound Bed of a Resected Sarcoma.

Gurtej Singh, Omer Kaymakcalan, Thomas R Hays, Adam Abbas, Sruthi Sridevan, Jasleen Kaur, Sourish Rathi, Jocellie Marquez, Soosan Ghazizadeh, Felix Tavernier and 5 more

Abstract read
In one paragraph

Article in Plastic and reconstructive surgery. Global open, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

15 authors.

Gurtej SinghFrom the Division of Plastic and Reconstructive Surgery, Department of Surgery, Stony Brook University Hospital and Medical Center, Stony Brook, NY.
Omer KaymakcalanFrom the Division of Plastic and Reconstructive Surgery, Department of Surgery, Stony Brook University Hospital and Medical Center, Stony Brook, NY.
Thomas R HaysOrlando Health at Orlando Regional Medical Center, Orlando, FL.
Adam AbbasStony Brook University, Stony Brook, NY.
Sruthi SridevanStony Brook University, Stony Brook, NY.
Jasleen KaurStony Brook University, Stony Brook, NY.
Sourish RathiStony Brook University, Stony Brook, NY.
Jocellie MarquezFrom the Division of Plastic and Reconstructive Surgery, Department of Surgery, Stony Brook University Hospital and Medical Center, Stony Brook, NY.
Soosan GhazizadehDepartment of Oral Biology and Pathology, Stony Brook University, Stony Brook, NY.
Felix TavernierDepartment of Pathology, Stony Brook University Hospital and Medical Center, Stony Brook, NY.
Brendan F BoyceDepartment of Pathology, Stony Brook University Hospital and Medical Center, Stony Brook, NY.
Sami U KhanFrom the Division of Plastic and Reconstructive Surgery, Department of Surgery, Stony Brook University Hospital and Medical Center, Stony Brook, NY.
Fazel A KhanDepartment of Orthopaedics, Stony Brook University Hospital and Medical Center, Stony Brook, NY.
Duc T BuiFrom the Division of Plastic and Reconstructive Surgery, Department of Surgery, Stony Brook University Hospital and Medical Center, Stony Brook, NY.
Alexander B DagumFrom the Division of Plastic and Reconstructive Surgery, Department of Surgery, Stony Brook University Hospital and Medical Center, Stony Brook, NY.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: One reason for local recurrence is the presence of positive surgical margins after tumor resection. An animal model accurately representing the microtumor burden will improve our understanding of these surgical margins. Using a rat model, we report a new methodology for creating microscopic tumors. Methods: Four different cell densities (1000, 10,000, 100,000, and 500,000 cells) of virus-induced Rous sarcoma XC cells (ATCC CCL-165) were topically added to 1.0 cm × 1.0 cm full-thickness wounds of male Rowett nude rats. Both Tegaderm and Tensoplast were then used to dress the wounds. After 9 days, the wound beds were excised, stained with hematoxylin and eosin, and analyzed using National Institutes of Health Image J software. Results: Better healing of the wound beds was observed for the smaller 2 cell densities (1000 and 10,000) as opposed to the higher 2 densities (100,000 and 500,000). The 2 higher cell density groups had gross identifiable tumors that extended deep through the dermis. On the other hand, the smaller cell density groups had microscopic tumor masses. Inflammation was present in all groups irrespective of the initial tumor cell densities, whereas hemorrhage was present only in the 2 higher cell density groups. Conclusions: This methodology can create a clinically relevant scenario of positive surgical margins after tumor resection. This induction method is simple, reasonably quick to use, and requires minimal surgical expertise. This approach could also develop microscopically positive margins for a much more comprehensive array of cancers.

Identifiers

PMID39619119
PMCPMC11608645

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.