Evidence map›Paper›PMID 28693163›Full record

ArticleOncology letters2017

Monocyte chemoattractant protein 1 expression and proliferation in primary central nervous system lymphoma.

Yoshinobu Takahashi, Takahiro Sawada, Toshiaki Akahane, Yumiko Kawase, Hidetoshi Ikeda, Keishi Makino, Hideo Nakamura, Takuichiro Hide, Shigetoshi Yano, Naoya Hashimoto and 1 more

Open access · diamondAbstract read
In one paragraph

Article in Oncology letters, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.5field-weighted citation impact, top 32% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Review
  3. 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

11 authors at 4 institutions in 1 country.

Yoshinobu TakahashiDepartment of Neurosurgery, Hokuto Hospital, Obihiro, Hokkaido 080-0033, Japan.
Takahiro SawadaDepartment of Cancer Biology and Genetics, Hokuto Hospital, Obihiro, Hokkaido 080-0033, Japan.
Toshiaki AkahaneDepartment of Pathology, Hokuto Hospital, Obihiro, Hokkaido 080-0033, Japan.
Yumiko KawaseDepartment of Cancer Biology and Genetics, Hokuto Hospital, Obihiro, Hokkaido 080-0033, Japan.
Hidetoshi IkedaDepartment of Neurosurgery, Osaka City General Hospital, Osaka 534-0021, Japan.
Keishi MakinoDepartment of Neurosurgery, Graduate School of Medical Science, Kumamoto University, Kumamoto 860-8556, Japan.
Hideo NakamuraDepartment of Neurosurgery, Graduate School of Medical Science, Kumamoto University, Kumamoto 860-8556, Japan.
Takuichiro HideDepartment of Neurosurgery, Graduate School of Medical Science, Kumamoto University, Kumamoto 860-8556, Japan.
Shigetoshi YanoDepartment of Neurosurgery, Graduate School of Medical Science, Kumamoto University, Kumamoto 860-8556, Japan.
Naoya HashimotoDepartment of Neurosurgery, Kyoto Prefectural University of Medicine, Kyoto, Japan.
Hajime KamadaDepartment of Neurosurgery, Hokuto Hospital, Obihiro, Hokkaido 080-0033, Japan.
Hokuto Hospital · JPKumamoto University · JPKyoto Prefectural University of Medicine · JPOsaka City General Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Whether the poor prognosis of primary central nervous system lymphoma (PCNSL) compared with systemic diffuse large B cell lymphoma (DLBCL) is attributable to the immune privilege of the intracerebral location or to intrinsic differences in the biological characteristics of two types of lymphoma remains unclear. Monocyte chemoattractant protein 1 (MCP-1) is essential to support tumor cell survival and growth, and the present study aimed to compare MCP-1 expression in PCNSL and peripheral DLBCL. The present study included 19 patients with PCNSL and 16 patients with DLBCL, all of whom had tissue diagnosis and lymphoma tissue samples available for analysis. Histology included immunohistochemistry using antibodies against a panel of lymphoma markers, antibodies specific to MCP-1, and antibodies specific to tumor-associated macrophages. MCP-1 expression was quantified using immunostaining scoring. RNA extraction and reverse transcription-quantitative polymerase chain reaction were used to determine

Indexed as

autocrinemonocyte chemoattractant protein 1primary central nervous system lymphomaproliferation

Identifiers

PMID28693163
PMCPMC5494900
OpenAlexW2610246046

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.