Evidence map›Paper›PMID 24376714›Full record

ArticlePloS one2013

Identification of biological properties of intralymphatic tumor related to the development of lymph node metastasis in lung adenocarcinoma.

Keisuke Kirita, Genichiro Ishii, Rie Matsuwaki, Yuki Matsumura, Shigeki Umemura, Shingo Matsumoto, Kiyotaka Yoh, Seiji Niho, Koichi Goto, Hironobu Ohmatsu and 3 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.8field-weighted citation impact, top 27% 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

11 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. 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

13 authors at 2 institutions in 1 country.

Keisuke KiritaPathology Division, Research Center for Innovative Oncology, National Cancer Center Hospital East, Chiba, Japan ; Division of Thoracic Oncology, National Cancer Center Hospital East, Chiba, Japan ; Juntendo University Graduate School of Medicine, Tokyo, Japan.
Genichiro IshiiPathology Division, Research Center for Innovative Oncology, National Cancer Center Hospital East, Chiba, Japan.
Rie MatsuwakiPathology Division, Research Center for Innovative Oncology, National Cancer Center Hospital East, Chiba, Japan ; Division of Thoracic Surgery, National Cancer Center Hospital East, Chiba, Japan.
Yuki MatsumuraDivision of Thoracic Surgery, National Cancer Center Hospital East, Chiba, Japan.
Shigeki UmemuraDivision of Thoracic Oncology, National Cancer Center Hospital East, Chiba, Japan.
Shingo MatsumotoDivision of Thoracic Oncology, National Cancer Center Hospital East, Chiba, Japan.
Kiyotaka YohDivision of Thoracic Oncology, National Cancer Center Hospital East, Chiba, Japan.
Seiji NihoDivision of Thoracic Oncology, National Cancer Center Hospital East, Chiba, Japan.
Koichi GotoDivision of Thoracic Oncology, National Cancer Center Hospital East, Chiba, Japan.
Hironobu OhmatsuDivision of Thoracic Oncology, National Cancer Center Hospital East, Chiba, Japan.
Yuichiro OheDivision of Thoracic Oncology, National Cancer Center Hospital East, Chiba, Japan ; Juntendo University Graduate School of Medicine, Tokyo, Japan.
Kanji NagaiDivision of Thoracic Surgery, National Cancer Center Hospital East, Chiba, Japan.
Atsushi OchiaiPathology Division, Research Center for Innovative Oncology, National Cancer Center Hospital East, Chiba, Japan.
National Cancer Center Hospital East · JPJuntendo University Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIntralymphatic tumors in the extratumoral area are considered to represent the preceding phase of lymph node metastasis. The aim of this study was to clarify the biological properties of intralymphatic tumors susceptible to the development of lymph node metastasis, with special reference to the expression of cancer initiating/stem cell (CIC/CSC) related markers in cancer cells and the number of infiltrating stromal cells. MATERIAL AND

methodsPrimary lung adenocarcinomas with lymphatic permeation in the extratumoral area were retrospectively examined (n = 107). We examined the expression levels of CIC/CSC related markers including ALDH1, OCT4, NANOG, SOX2 and Caveolin-1 in the intralymphatic cancer cells to evaluate their relationship to lymph node metastasis. Moreover, the number of infiltrating stromal cells expressing CD34, α-smooth muscle actin, and CD204 were also evaluated.

resultsAmong the intralymphatic tissues, low ALDH1 expression in cancer cells, high SOX2 expression in cancer cells, and a high number of CD204(+) macrophages were independent predictive factors for lymph node metastasis (P = 0.004, P = 0.008, and P = 0.028, respectively). Among these factors, only low ALDH1 expression in cancer cells was significantly correlated with the farther spreading of lymph node metastasis (mediastinal lymph node, pathological N2) (P = 0.046) and the metastatic lymph node ratio (metastatic/resected) (P = 0.028). On the other hand, in the primary tumors, ALDH1 expression in the cancer cells was not associated with lymph node metastasis. Intralymphatic cancer cells expressing low ALDH1 levels exhibited lower E-cadherin expression levels than cancer cells with high levels of ALDH1 expression (P = 0.015).

conclusionsIntralymphatic cancer cells expressing low levels of ALDH1 and infiltrating macrophages expressing CD204 have a critical impact on lymph node metastasis. Our study also highlighted the significance of evaluating the biological properties of intralymphatic tumors for tumor metastasis.

Indexed as

AdenocarcinomaAdenocarcinoma of LungAdultAgedAged, 80 and overAldehyde Dehydrogenase 1 FamilyCadherinsFemaleGene Expression Regulation, NeoplasticHumansIsoenzymesLung NeoplasmsLymphatic MetastasisMacrophagesMaleMiddle AgedAldehyde Dehydrogenase 1 FamilyALDH1A1 protein, humanCadherinsIsoenzymesMSR1 protein, humanRetinal DehydrogenaseScavenger Receptors, Class ASOX2 protein, humanSOXB1 Transcription Factors

Identifiers

PMID24376714
PMCPMC3871680
OpenAlexW2032261911

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.