Evidence map›Paper›PMID 32326109›Full record

ArticleCancers2020

Expansion of Circulating Tumor Cells from Patients with Locally Advanced Pancreatic Cancer Enable Patient Derived Xenografts and Functional Studies for Personalized Medicine.

Lianette Rivera-Báez, Ines Lohse, Eric Lin, Shreya Raghavan, Sarah Owen, Ramdane Harouaka, Kirk Herman, Geeta Mehta, Theodore S Lawrence, Meredith A Morgan and 2 more

Abstract read
In one paragraph

Article in Cancers, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing 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

22 citing papers in PubMed.

  1. Article
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  15. Article
  16. Technologies for Viable Circulating Tumor Cell Isolation.International journal of molecular sciences · 2022
    Review
  17. Article
  18. Article
  19. Article
  20. 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

12 authors.

Lianette Rivera-BáezDepartment of Chemical Engineering, University of Michigan, Ann Arbor, MI 48105, USA.
Ines LohseDepartment of Radiation Oncology, University of Michigan Medical School, Ann Arbor, MI 48109, USA.
Eric LinDepartment of Chemical Engineering, University of Michigan, Ann Arbor, MI 48105, USA.
Shreya RaghavanDepartment of Materials Science and Engineering, University of Michigan, Ann Arbor, MI 48109, USA.ORCID 0000-0002-4631-7762
Sarah OwenDepartment of Chemical Engineering, University of Michigan, Ann Arbor, MI 48105, USA.ORCID 0000-0002-4102-7707
Ramdane HarouakaDepartment of Internal Medicine, University of Michigan Comprehensive Cancer Center, Ann Arbor, MI 48109, USA.ORCID 0000-0002-1425-3960
Kirk HermanDepartment of Radiation Oncology, University of Michigan Medical School, Ann Arbor, MI 48109, USA.
Geeta MehtaBiointerfaces Institute, University of Michigan, Ann Arbor, MI 48105, USA.ORCID 0000-0001-5967-6425
Theodore S LawrenceDepartment of Internal Medicine, University of Michigan Comprehensive Cancer Center, Ann Arbor, MI 48109, USA.
Meredith A MorganDepartment of Radiation Oncology, University of Michigan Medical School, Ann Arbor, MI 48109, USA.
Kyle C CuneoDepartment of Radiation Oncology, University of Michigan Medical School, Ann Arbor, MI 48109, USA.
Sunitha NagrathDepartment of Chemical Engineering, University of Michigan, Ann Arbor, MI 48105, USA.ORCID 0000-0002-1497-7977

Funding

Sensitization to Chemoradiation by Therapeutic Targeting of the DNA Damage ResponseU01CA216449 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LAWRENCE, THEODORE S · 2017 to 2021
$3.0M
Targeting the DNA damage response in combination with radiation to induce innate immunity and improve immunotherapy efficacy in pancreatic cancerR01CA240515 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MORGAN, MEREDITH A · 2020 to 2024
$2.2M
NCI NIH HHS R01 CA240515NCI NIH HHS U01 CA216449NIH HHS R01-CA-208335-01
6 · The paper itself

Abstract

Improvement in pancreatic cancer treatment represents an urgent medical goal that has been hampered by the lack of predictive biomarkers. Circulating Tumor Cells (CTCs) may be able to overcome this issue by allowing the monitoring of therapeutic response and tumor aggressiveness through ex vivo expansion. The successful expansion of CTCs is challenging, due to their low numbers in blood and the high abundance of blood cells. Here, we explored the utility of pancreatic CTC cultures as a preclinical model for treatment response. CTCs were isolated from ten patients with locally advanced pancreatic cancer using the Labyrinth, a biomarker independent, size based, inertial microfluidic separation device. Three patient-derived CTC samples were successfully expanded in adherent and spheroid cultures. Molecular and functional characterization was performed on the expanded CTC lines. CTC lines exhibited KRAS mutations, consistent with pancreatic cancers. Additionally, we evaluated take rate and metastatic potential in vivo and examined the utility of CTC lines for cytotoxicity assays. Patient derived expanded CTCs successfully generated patient derived xenograft (PDX) models with a 100% take rate. Our results demonstrate that CTC cultures are possible and provide a valuable resource for translational pancreatic cancer research, while also providing meaningful insight into the development of distant metastasis, as well as treatment resistance.

Indexed as

biomarkerscirculating tumor cellspancreatic cancerpersonalized medicine

Identifiers

PMID32326109
PMCPMC7225920

What OpenQuestion holds

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Registered trials

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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.