Evidence map›Paper›PMID 36625629›Full record

ArticleAdvanced healthcare materials2023

Live Cell Lineage Tracing of Dormant Cancer Cells.

Hyuna Kim, Anna Wirasaputra, Farnaz Mohammadi, Aritra Nath Kundu, Jennifer A E Esteves, Laura M Heiser, Aaron S Meyer, Shelly R Peyton

Open access · greenAbstract read
In one paragraph

Article in Advanced healthcare materials, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

10 citing papers in PubMed, 14 citations in OpenAlex.

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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

8 authors at 3 institutions in 1 country.

Hyuna KimMolecular and Cell Biology Graduate Program, University of Massachusetts, Amherst, MA, 01002, USA.ORCID 0000-0001-6954-6595
Anna WirasaputraDepartment of Chemical Engineering, University of Massachusetts, Amherst, MA, 01002, USA.
Farnaz MohammadiDepartment of Bioengineering, University of California, Los Angeles, CA, 90095, USA.
Aritra Nath KunduDepartment of Chemical Engineering, University of Massachusetts, Amherst, MA, 01002, USA.
Jennifer A E EstevesDepartment of Biomedical Engineering, University of Massachusetts, Amherst, MA, 01002, USA.ORCID 0000-0002-5839-5995
Laura M HeiserDepartment of Biomedical Engineering, Knight Cancer Institute, Oregon Health & Science University, Portland, OR, 97239, USA.
Aaron S MeyerDepartment of Bioengineering, University of California, Los Angeles, CA, 90095, USA.
Shelly R PeytonMolecular and Cell Biology Graduate Program, University of Massachusetts, Amherst, MA, 01002, USA.ORCID 0000-0002-6108-8056
University of Massachusetts Amherst · USUniversity of California, Los Angeles · USOregon Health & Science University · US

Funding

Understanding the Impact of Microscale and Nanoscale Heterogeneity and ResistanceU54CA209988 · NCI · OREGON HEALTH & SCIENCE UNIVERSITY · PI GRAY, JOE W. · 2017 to 2021
$10.3M
Biotechnology Training Program in Applied Life SciencesT32GM135096 · NIGMS · UNIVERSITY OF MASSACHUSETTS AMHERST · PI Jeanne Ann Hardy, Ashish A. Kulkarni · 2020 to 2026
$3.9M
Tissue-specific stem cells and breast cancer tissue tropism in bioengineered microenvironmentsDP2CA186573 · NCI · UNIVERSITY OF MASSACHUSETTS AMHERST · PI PEYTON, SHELLY R. · 2013 to 2015
$2.6M
Personalization and Failure Testing of Dual Switch Gene Drives in Lung CancerU01CA265709 · NCI · PENNSYLVANIA STATE UNIVERSITY, THE · PI PRITCHARD, JUSTIN · 2021 to 2025
$2.6M
Precision lung cancer therapy design through multiplexed adapter measurementU01CA215709 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI HAURA, ERIC B., MEYER, AARON SAMUEL · 2017 to 2021
$2.3M
A Synthetic Bone Marrow to Understand Breast Cancer DormancyR21CA223783 · NCI · UNIVERSITY OF MASSACHUSETTS AMHERST · PI PEYTON, SHELLY R. · 2018 to 2019
$350k
NCI NIH HHS DP2 CA186573NCI NIH HHS R21 CA223783NCI NIH HHS U01 CA215709NCI NIH HHS U01 CA265709NCI NIH HHS U54 CA209988NIGMS NIH HHS T32 GM135096
6 · The paper itself

Abstract

Breast cancer is a leading cause of global cancer-related deaths, and metastasis is the overwhelming culprit of poor patient prognosis. The most nefarious aspect of metastasis is dormancy, a prolonged period between primary tumor resection and relapse. Current therapies are insufficient at killing dormant cells; thus, they can remain quiescent in the body for decades until eventually undergoing a phenotypic switch, resulting in metastases that are more adaptable and drug resistant. Unfortunately, dormancy has few in vitro models, largely because lab-derived cell lines are highly proliferative. Existing models address tumor dormancy, not cellular dormancy, because tracking individual cells is technically challenging. To combat this problem, a live cell lineage approach to find and track individual dormant cells, distinguishing them from proliferative and dying cells over multiple days, is adapted. This approach is applied across a range of different in vitro microenvironments. This approach reveals that the proportion of cells that exhibit long-term quiescence is regulated by both cell intrinsic and extrinsic factors, with the most dormant cells found in 3D collagen gels. This paper envisions that this approach will prove useful to biologists and bioengineers in the dormancy community to identify, quantify, and study dormant tumor cells.

Indexed as

Breast NeoplasmsCell LineageFemaleHumansTumor Microenvironmentbiomaterialsbreast cancercollagenMatrigelpoly(ethylene glycol) hydrogels

Identifiers

PMID36625629
PMCPMC10238615
OpenAlexW4315436574

What OpenQuestion holds

Textmetadata
LicenceTDM
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.