Evidence map›Paper›PMID 25819560›Full record

ArticleScientific reports2015

The extent of inflammatory infiltration in primary cancer tissues is associated with lymphomagenesis in immunodeficient mice.

Lianhai Zhang, Yiqiang Liu, Xiaohong Wang, Zhiyu Tang, Shuangxi Li, Ying Hu, Xianglong Zong, Xiaojiang Wu, Zhaode Bu, Aiwen Wu and 10 more

Abstract read
In one paragraph

Article in Scientific reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
–field-weighted citation impact
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

30 citing papers in PubMed.

  1. Article
  2. Article
  3. Cancer Stem Cells from Definition to Detection and Targeted Drugs.International journal of molecular sciences · 2024
    Review
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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

20 authors.

Lianhai ZhangKey laboratory of Carcinogenesis and Translational Research (Ministry of Education), Department of Surgery, Peking University Cancer Hospital and Institute, Beijing, China.
Yiqiang LiuDepartment of Pathology, Peking University Cancer Hospital and Institute, Beijing, China.
Xiaohong WangKey laboratory of Carcinogenesis and Translational Research (Ministry of Education), Department of Surgery, Peking University Cancer Hospital and Institute, Beijing, China.
Zhiyu TangBeiGene (Beijing) Co. Ltd, No. 30 Science Park Road, Life Science Park, Changping District, Beijing, China.
Shuangxi LiKey laboratory of Carcinogenesis and Translational Research (Ministry of Education), Department of Surgery, Peking University Cancer Hospital and Institute, Beijing, China.
Ying HuKey laboratory of Carcinogenesis and Translational Research (Ministry of Education), Department of Surgery, Peking University Cancer Hospital and Institute, Beijing, China.
Xianglong ZongKey laboratory of Carcinogenesis and Translational Research (Ministry of Education), Department of Surgery, Peking University Cancer Hospital and Institute, Beijing, China.
Xiaojiang WuKey laboratory of Carcinogenesis and Translational Research (Ministry of Education), Department of Surgery, Peking University Cancer Hospital and Institute, Beijing, China.
Zhaode BuKey laboratory of Carcinogenesis and Translational Research (Ministry of Education), Department of Surgery, Peking University Cancer Hospital and Institute, Beijing, China.
Aiwen WuKey laboratory of Carcinogenesis and Translational Research (Ministry of Education), Department of Surgery, Peking University Cancer Hospital and Institute, Beijing, China.
Ziyu LiKey laboratory of Carcinogenesis and Translational Research (Ministry of Education), Department of Surgery, Peking University Cancer Hospital and Institute, Beijing, China.
Zhongwu LiDepartment of Pathology, Peking University Cancer Hospital and Institute, Beijing, China.
Xiaozheng HuangDepartment of Pathology, Peking University Cancer Hospital and Institute, Beijing, China.
Ling JiaDepartment of Pathology, Peking University Cancer Hospital and Institute, Beijing, China.
Qiang KangDepartment of Pathology, Peking University Cancer Hospital and Institute, Beijing, China.
Yong LiuBeiGene (Beijing) Co. Ltd, No. 30 Science Park Road, Life Science Park, Changping District, Beijing, China.
David SuttonBeiGene (Beijing) Co. Ltd, No. 30 Science Park Road, Life Science Park, Changping District, Beijing, China.
Lai WangBeiGene (Beijing) Co. Ltd, No. 30 Science Park Road, Life Science Park, Changping District, Beijing, China.
Lusong LuoBeiGene (Beijing) Co. Ltd, No. 30 Science Park Road, Life Science Park, Changping District, Beijing, China.
Jiafu JiKey laboratory of Carcinogenesis and Translational Research (Ministry of Education), Department of Surgery, Peking University Cancer Hospital and Institute, Beijing, China.

Funding

Impact of Prenatal Alcohol Exposure on Receptor Targeting and FunctioningR03AA020101 · NIAAA · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI CALDWELL, KEVIN K. · 2010 to 2011
$148k
NIAAA NIH HHS R03 AA020101
6 · The paper itself

Abstract

Xenotransplantation of human cancers into immunodeficient mice is a very useful approach for studying human tumor biology. However, the occasional occurrence of lymphomagenesis in some mice can spoil the model and must be investigated in detail. We found that a high percentage (32.5%, 26/80) of cancer patient-derived xenografts (PDXs) resembled lymphoma in NOD/SCID mice. Of the 26 xenografts, 23 were human-derived expressing human CD45 (hCD45+) and proved to be of the B-cell subtype (CD3-/CD20+), and they were all positive for Epstein-Barr virus (EBV). The remaining 3 xenografts proved to be mouse-derived for both hCD45- and negative amplification of a human gene. The most interesting finding is that gastric cancer had much higher rates (24/126, 19.0%) of lymphoma formation in the PDX model than did colorectal cancer (1/43, 2.3%). Statistical analysis revealed that cancer type and inflammation in the parent tumor are significantly associated with lymphomagenesis. Further validation discovered lymphomagenesis by inoculating only gastritis mucosa. Therefore, our findings suggest that it is necessary to take precautions when directly xenografting cancer tissues with remarkable baseline inflammation, such as gastric cancer into immunodeficient NOD/SCID strains. Further, the established xenograft models should be validated by both leukocyte markers and human gene signatures.

Indexed as

AnimalsB-LymphocytesCarcinogenesisDisease Models, AnimalEpstein-Barr Virus InfectionsHerpesvirus 4, HumanHumansInflammationLeukocyte Common AntigensLymphomaLymphoma, B-CellMiceMice, Inbred NODMice, SCIDTransplantation, HeterologousLeukocyte Common AntigensPTPRC protein, human

Identifiers

PMID25819560
PMCPMC4377553

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Registered trials

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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.