Evidence map›Paper›PMID 23532368›Full record

ArticleInternational journal of medical sciences2013

Tumor-infiltrating immune cells: triggers for tumor capsule disruption and tumor progression?

Bin Jiang, Jeffrey Mason, Anahid Jewett, Min-ling Liu, Wen Chen, Jun Qian, Yijiang Ding, Shuqing Ding, Min Ni, Xichen Zhang and 1 more

Open access · goldAbstract read
In one paragraph

Article in International journal of medical sciences, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
1.2field-weighted citation impact, top 22% 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

16 citing papers in PubMed, 1 synthesis or guideline pooled it, 37 citations in OpenAlex.

  1. Pooled it
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  12. Prognostic significance of tumor-infiltrating lymphocytes in ductal carcinoma in situ of the breast.Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc · 2018
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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 1 institution in 1 country.

Bin JiangNational Medical Centre of Colorectal Disease, The Third Affiliated Hospital, Nanjing University of Traditional Chinese Medicine TCM, Nanjing, China. jbfirsth@yahoo.com.cn
Jeffrey Mason
Anahid Jewett
Min-ling Liu
Wen Chen
Jun Qian
Yijiang Ding
Shuqing Ding
Min Ni
Xichen Zhang
Yan-gao Man
Nanjing Traditional Chinese Medicine Hospital · CN

Funding

Inactivation of Cytotoxic Effectors in Oral CarcinomasR01DE012880 · NIDCR · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI JEWETT, ANAHID · 2001 to 2003
$718k
Technology to improve the assessment of tissue-associated protein biomarkersI01BX001092 · VA · BALTIMORE VA MEDICAL CENTER · PI MASON, JEFFREY THOMAS · 2013 to 2017
–
BLRD VA I01 BX001092NIDCR NIH HHS R01 DE012880NIDCR NIH HHS R01-DE12880
6 · The paper itself

Abstract

backgroundOur previous studies of human breast and prostate cancer have shown that aberrant immune cell infiltration is associated with focal tumor capsule disruption and tumor cell budding that facilitate invasion and metastasis. Our current study attempted to determine whether aberrant immune cell infiltration would have similar impact on colorectal cancer (CRC). MATERIALS AND

methodsTissue sections from 100 patients with primary CRC were assessed for the frequencies of focal basement membrane (BM) disruption, muscularis mucosa (MM) fragmentation, and tumor cell dissemination in epithelial structures adjacent and distal to infiltrating lymphoid aggregates using a panel of biomarkers and quantitative digital imaging.

resultsOur study revealed: (1) epithelial structures adjacent to lymphoid follicles or aggregates had a significantly higher (p<0.001) frequency of focally disrupted BM, dissociated epithelial cells in the stroma, disseminated epithelial cells within lymphatic ducts or blood vessels, and fragmented MM than their distal counterparts, (2) a majority of dissociated epithelial cells within the stroma or vascular structures were immediately subjacent to or physically associated with infiltrating immune cells, (3) the junctions of pre-invasive and invasive lesions were almost exclusively located at sites adjacent to lymphoid follicles or aggregates, (4) infiltrating immune cells were preferentially associated with epithelial capsules that show distinct degenerative alterations, and (5) infiltrating immune cells appeared to facilitate tumor stem cell proliferation, budding, and dissemination.

conclusionsAberrant immune cell infiltration may have the same destructive impact on the capsule of all epithelium-derived tumors. This, in turn, may selectively favor the proliferation of tumor stem or progenitor cells overlying these focal disruptions. These proliferating epithelial tumor cells subsequently disseminate from the focal disruption leading to tumor invasion and metastasis.

Indexed as

Cell ProliferationNeoplasm InvasivenessBiomarkers, TumorCell AggregationColorectal NeoplasmsEpithelial CellsFemaleHumansLeukocytesLymphocytesMaleMiddle AgedNeoplasm MetastasisBiomarkers, TumorColorectal cancermetastasis, lymphocyte aggregates.tumor capsuletumor invasion

Identifiers

PMID23532368
PMCPMC3607233
OpenAlexW2028292569

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.