Evidence map›Paper›PMID 28860411›Full record

ArticleThe oncologist2018

Improved Detection of Circulating Epithelial Cells in Patients with Intraductal Papillary Mucinous Neoplasms.

Joseph W Franses, Omer Basar, Abdurrahman Kadayifci, Osman Yuksel, Melissa Choz, Anupriya S Kulkarni, Eric Tai, Kevin D Vo, Kshitij S Arora, Niyati Desai and 7 more

Erratum issuedOpen access · bronzeAbstract read
In one paragraph

Article in The oncologist, 2018. 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 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.2field-weighted citation impact, top 19% 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

18 citing papers in PubMed, 31 citations in OpenAlex.

  1. Review
  2. Observational
  3. Article
  4. Article
  5. How much do we know about the metastatic process?Clinical & experimental metastasis · 2024
    Review
  6. Article
  7. Review
  8. Clinical and Molecular Attributes and Evaluation of Pancreatic Cystic Neoplasm.Biochimica et biophysica acta. Reviews on cancer · 2023
    Review
  9. Review
  10. Exploring the Clinical Utility of Pancreatic Cancer Circulating Tumor Cells.International journal of molecular sciences · 2022
    Review
  11. Review
  12. Circulating tumor cells in the early detection of human cancers.International journal of biological sciences · 2022
    Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. In Reply.The oncologist · 2018
    Article
  18. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors at 3 institutions in 1 country.

Joseph W FransesCancer Center, Massachusetts General Hospital, Boston, Massachusetts, USA.
Omer BasarDivision of Gastroenterology, Massachusetts General Hospital, Boston, Massachusetts, USA.
Abdurrahman KadayifciDivision of Gastroenterology, Massachusetts General Hospital, Boston, Massachusetts, USA.
Osman YukselDivision of Gastroenterology, Massachusetts General Hospital, Boston, Massachusetts, USA.
Melissa ChozCancer Center, Massachusetts General Hospital, Boston, Massachusetts, USA.
Anupriya S KulkarniCancer Center, Massachusetts General Hospital, Boston, Massachusetts, USA.
Eric TaiCancer Center, Massachusetts General Hospital, Boston, Massachusetts, USA.
Kevin D VoCancer Center, Massachusetts General Hospital, Boston, Massachusetts, USA.
Kshitij S AroraCancer Center, Massachusetts General Hospital, Boston, Massachusetts, USA.
Niyati DesaiCancer Center, Massachusetts General Hospital, Boston, Massachusetts, USA.
Joseph A LicausiCancer Center, Massachusetts General Hospital, Boston, Massachusetts, USA.
Mehmet TonerCenter for Engineering in Medicine, Massachusetts General Hospital, Boston, Massachusetts, USA.
Shyamala MaheswaranCancer Center, Massachusetts General Hospital, Boston, Massachusetts, USA.
Daniel A HaberCancer Center, Massachusetts General Hospital, Boston, Massachusetts, USA.
David P RyanCancer Center, Massachusetts General Hospital, Boston, Massachusetts, USA.
William R BruggeDivision of Gastroenterology, Massachusetts General Hospital, Boston, Massachusetts, USA brugge.william@mgh.harvard.edu dting1@mgh.harvard.edu.
David T TingCancer Center, Massachusetts General Hospital, Boston, Massachusetts, USA brugge.william@mgh.harvard.edu dting1@mgh.harvard.edu.
Massachusetts General Hospital · USHarvard University · USHoward Hughes Medical Institute · US

Funding

Point-of care Microfluidics for Early Detection of CancerU01EB012493 · NIBIB · MASSACHUSETTS GENERAL HOSPITAL · PI HABER, DANIEL A., TONER, MEHMET · 2010 to 2018
$19.6M
Dana Farber/Harvard Cancer Consortium Career Development Program in Clinical OncologyK12CA087723 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI David Tsai Ting · 2002 to 2026
$17.9M
Modeling Metastasis and Acquired Drug Resistance Using Circulating Tumor CellsR01CA129933 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI Daniel A. Haber · 2008 to 2026
$7.5M
Howard Hughes Medical InstituteNCI NIH HHS K12 CA087723NCI NIH HHS R01 CA129933NIBIB NIH HHS U01 EB012493
6 · The paper itself

Abstract

backgroundRecent work has demonstrated early shedding of circulating epithelial cells (CECs) from premalignant intraductal papillary mucinous neoplasms (IPMNs). However, the potential use of CECs as a "liquid biopsy" for patients with IPMNs has been limited by antigen dependence of CEC isolation devices and the lack of robust detection biomarkers across CEC phenotypes. MATERIALS AND

methodsWe utilized a negative depletion microfluidic platform to purify CECs from contaminating leukocytes and coupled this platform with immunofluorescence, RNA in situ hybridization, and RNA sequencing (RNA-seq) detection and enumeration.

resultsUsing established protein (EpCAM, cytokeratins) and novel noncoding RNA (HSATII, cytokeratins) biomarkers, we detected CECs in 88% of patients bearing IPMN lesions. RNA-seq analysis for MUC genes confirm the likely origin of these CECs from pancreatic lesions.

conclusionOur findings increase the sensitivity of detection of these cells and therefore could have clinical implications for cancer risk stratification. IMPLICATIONS FOR PRACTICE: This work describes a high-sensitivity platform for detection of epithelial cells shed from preneoplastic lesions at high risk of malignant transformation. Further research efforts are underway to define the transcriptional programs that might allow discrimination between circulating cells released from tumors that will become malignant and cells released from tumors that will not. After further refinement, this combination of technologies could be deployed for monitoring and early detection of patients at high risk for developing new or recurrent pancreatic malignancies.

Indexed as

Adenocarcinoma, MucinousAdultAgedAged, 80 and overCarcinoma, Pancreatic DuctalCarcinoma, PapillaryCase-Control StudiesEpithelial CellsFemaleFollow-Up StudiesHumansMaleMiddle AgedNeoplastic Cells, CirculatingPancreatic NeoplasmsPrecancerous ConditionsCirculating epithelial cellsEarly detectionPancreatic cancer

Identifiers

PMID28860411
PMCPMC5759811
OpenAlexW2753147780

What OpenQuestion holds

Textmetadata
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.