Evidence map›Paper›PMID 31024520›Full record

ArticleFrontiers in immunology2019

Defective Localization With Impaired Tumor Cytotoxicity Contributes to the Immune Escape of NK Cells in Pancreatic Cancer Patients.

Seon Ah Lim, Jungwon Kim, Seunghyun Jeon, Min Hwa Shin, Joonha Kwon, Tae-Jin Kim, Kyungtaek Im, Youngmin Han, Wooil Kwon, Sun-Whe Kim and 4 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 80 papers.

0numbers the graph read from it
0cells of the map it votes in
80citing papers in PubMed
4.3field-weighted citation impact, top 5% 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

80 citing papers in PubMed, 102 citations in OpenAlex.

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20 more citing papers are in PubMed but not listed here.

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

14 authors at 4 institutions in 2 countries.

Seon Ah LimDepartment of Biochemistry and Molecular Biology, Korea University College of Medicine, Seoul, South Korea.
Jungwon KimDepartment of Biochemistry and Molecular Biology, Korea University College of Medicine, Seoul, South Korea.
Seunghyun JeonDepartment of Biochemistry and Molecular Biology, Korea University College of Medicine, Seoul, South Korea.
Min Hwa ShinDepartment of Biochemistry and Molecular Biology, Korea University College of Medicine, Seoul, South Korea.
Joonha KwonDepartment of Biochemistry and Molecular Biology, Korea University College of Medicine, Seoul, South Korea.
Tae-Jin KimDepartment of Biochemistry and Molecular Biology, Korea University College of Medicine, Seoul, South Korea.
Kyungtaek ImDepartment of Biochemistry and Molecular Biology, Korea University College of Medicine, Seoul, South Korea.
Youngmin HanDepartment of Surgery and Cancer Research Institute, Seoul National University Hospital, Seoul National University College of Medicine, Seoul, South Korea.
Wooil KwonDepartment of Surgery and Cancer Research Institute, Seoul National University Hospital, Seoul National University College of Medicine, Seoul, South Korea.
Sun-Whe KimDepartment of Surgery and Cancer Research Institute, Seoul National University Hospital, Seoul National University College of Medicine, Seoul, South Korea.
Cassian YeeDepartment of Melanoma Medical Oncology and Immunology, MD Anderson Cancer Center, Houston, TX, United States.
Seong-Jin KimPrecision Medicine Research Center, Advanced Institutes of Convergence Technology, Seoul National University, Suwon, South Korea.
Jin-Young JangDepartment of Surgery and Cancer Research Institute, Seoul National University Hospital, Seoul National University College of Medicine, Seoul, South Korea.
Kyung-Mi LeeDepartment of Biochemistry and Molecular Biology, Korea University College of Medicine, Seoul, South Korea.
Korea University · KRThe University of Texas MD Anderson Cancer Center · USSeoul National University Hospital · KRSeoul National University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tumor-infiltrating lymphocytes (TILs), found in patients with advanced pancreatic ductal adenocarcinoma (PDAC), are shown to correlate with overall survival (OS) rate. Although majority of TILs consist of CD8

Indexed as

AdenocarcinomaAgedCarcinoma, Pancreatic DuctalCell Line, TumorCell ProliferationFemaleHumansK562 CellsKiller Cells, NaturalLymphocytes, Tumor-InfiltratingMalePancreatic NeoplasmsPrognosisTumor EscapeTumor Microenvironmentcancer immunobiologycellular immunologychemokinesimmunotherapypancreatic cancer

Identifiers

PMID31024520
PMCPMC6465515
OpenAlexW2939238109

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.