Evidence map›Paper›PMID 36230499›Full record

ArticleCancers2022

Identification and Morphological Characterization of Features of Circulating Cancer-Associated Macrophage-like Cells (CAMLs) in Endometrial Cancers.

Raed Sulaiman, Pradip De, Jennifer C Aske, Xiaoqian Lin, Adam Dale, Ethan Vaselaar, Cheryl Ageton, Kris Gaster, Luis Rojas Espaillat, David Starks and 1 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.9field-weighted citation impact, top 27% 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

7 citing papers in PubMed, 11 citations in OpenAlex.

  1. Review
  2. Article
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  5. Article
  6. Cell Fusion and Syncytia Formation in Cancer.Results and problems in cell differentiation · 2024
    Review
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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 2 institutions in 1 country.

Raed SulaimanDepartment of Pathology, Avera Cancer Institute, Sioux Falls, SD 57105, USA.
Pradip DeTranslational Oncology Laboratory, Avera Research Institute, Sioux Falls, SD 57105, USA.
Jennifer C AskeTranslational Oncology Laboratory, Avera Research Institute, Sioux Falls, SD 57105, USA.ORCID 0000-0001-9405-5464
Xiaoqian LinTranslational Oncology Laboratory, Avera Research Institute, Sioux Falls, SD 57105, USA.
Adam DaleTranslational Oncology Laboratory, Avera Research Institute, Sioux Falls, SD 57105, USA.
Ethan VaselaarTranslational Oncology Laboratory, Avera Research Institute, Sioux Falls, SD 57105, USA.
Cheryl AgetonDepartment of Research Oncology, Avera Cancer Institute, Sioux Falls, SD 57105, USA.
Kris GasterOutpatient Cancer Clinics, Avera Cancer Institute, Sioux Falls, SD 57105, USA.
Luis Rojas EspaillatDepartment of Gynecologic Oncology, Avera Cancer Institute, Sioux Falls, SD 57105, USA.ORCID 0000-0003-2520-5873
David StarksDepartment of Gynecologic Oncology, Avera Cancer Institute, Sioux Falls, SD 57105, USA.
Nandini DeyTranslational Oncology Laboratory, Avera Research Institute, Sioux Falls, SD 57105, USA.ORCID 0000-0002-5533-8784
Avera Health · USUniversity of South Dakota · US

Funding

Avera McKennan Hospital & University Health Center NA
6 · The paper itself

Abstract

The blood of patients with solid tumors contains circulating tumor-associated cells, including epithelial cells originating from the tumor mass, such as circulating tumor cells (CTCs), or phagocytic myeloid cells (differentiated monocytes), such as circulating cancer-associated macrophage-like cells (CAMLs). We report for the first time the identification and in-depth morphologic characterization of CAMLs in patients with endometrial cancers. We isolated CAMLs by size-based filtration on lithographically fabricated membranes followed by immunofluorescence, using a CD45+/CK 8,18,19+/EpCAM+/CD31+/macrophage-like nuclear morphology, from > 70 patients. Irrespective of the histological and pathological parameters, 98% of patients were positive for CAMLs. Two size-based subtypes of CAMLs, <20 µm (tiny) and >20 µm (giant) CAMLs, of distinctive polymorphic morphologies with mononuclear or fused polynuclear structures in several morphological states were observed, including apoptotic CAMLs, CAML−WBC doublets, conjoined CAMLs, CAML−WBC clusters, and CTC−CAML−WBC clusters. In contrast, CAMLs were absent in patients with non-neoplastic/benign tumors, healthy donors, and leucopaks. Enumerating CTCs simultaneously from the same patient, we observed that CTC-positive patients are positive for CAMLs, while 55% out of all CAML-positive patients were found positive for CTCs. Our study demonstrated for the first time the distinctive morphological characteristics of endometrial CAMLs in the context of the presence of CTCs in patients.

Indexed as

CAMLsCTCendometrial cancersliquid biopsytriple immuno-fluorescence

Identifiers

PMID36230499
PMCPMC9558552
OpenAlexW4296991328

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.