Evidence map›Paper›PMID 31186031›Full record

ArticleDiagnostic pathology2019

Association of tumour-associated macrophages with cancer cell EMT, invasion, and metastasis of Kazakh oesophageal squamous cell cancer.

Jihong Liu, Chunxiao Li, Liyan Zhang, Kai Liu, Xianli Jiang, Xueli Wang, Lan Yang, Weihua Liang, Kunping Liu, Jianming Hu and 1 more

Open access · goldAbstract read
In one paragraph

Article in Diagnostic pathology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.4field-weighted citation impact, top 9% 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

15 citing papers in PubMed, 43 citations in OpenAlex.

  1. Review
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  5. Review
  6. HPV16 infection promotes an M2 macrophage phenotype to promote the invasion and metastasis of esophageal squamous cell carcinoma.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2021
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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 3 institutions in 1 country.

Jihong LiuDepartment of Anatomic and Surgical Pathology, and Key Laboratory of Xinjiang Endemic and Ethnic Diseses, The First Affiliated Hospital, Shihezi University School of Medicine, Xinjiang, 832002, People's Republic of China.
Chunxiao LiDepartment of Anatomic and Surgical Pathology, and Key Laboratory of Xinjiang Endemic and Ethnic Diseses, The First Affiliated Hospital, Shihezi University School of Medicine, Xinjiang, 832002, People's Republic of China.
Liyan ZhangDepartment of Neurology, Beijing Friendship Hospital,Capital Medical University, Beijing, 100020, People's Republic of China.
Kai LiuDepartment of Anatomic and Surgical Pathology, and Key Laboratory of Xinjiang Endemic and Ethnic Diseses, The First Affiliated Hospital, Shihezi University School of Medicine, Xinjiang, 832002, People's Republic of China.
Xianli JiangDepartment of Anatomic and Surgical Pathology, and Key Laboratory of Xinjiang Endemic and Ethnic Diseses, The First Affiliated Hospital, Shihezi University School of Medicine, Xinjiang, 832002, People's Republic of China.
Xueli WangDepartment of Anatomic and Surgical Pathology, and Key Laboratory of Xinjiang Endemic and Ethnic Diseses, The First Affiliated Hospital, Shihezi University School of Medicine, Xinjiang, 832002, People's Republic of China.
Lan YangDepartment of Anatomic and Surgical Pathology, and Key Laboratory of Xinjiang Endemic and Ethnic Diseses, The First Affiliated Hospital, Shihezi University School of Medicine, Xinjiang, 832002, People's Republic of China.
Weihua LiangDepartment of Anatomic and Surgical Pathology, and Key Laboratory of Xinjiang Endemic and Ethnic Diseses, The First Affiliated Hospital, Shihezi University School of Medicine, Xinjiang, 832002, People's Republic of China.
Kunping LiuDepartment of Pathology, The Sixth Affiliated Hospital of Guangzhou Medical University, Qingyuan People's Hospital, Qingyuan, Guangdong, 511518, People's Republic of China.
Jianming HuDepartment of Anatomic and Surgical Pathology, and Key Laboratory of Xinjiang Endemic and Ethnic Diseses, The First Affiliated Hospital, Shihezi University School of Medicine, Xinjiang, 832002, People's Republic of China. jianming.120@163.com.
Feng LiDepartment of Anatomic and Surgical Pathology, and Key Laboratory of Xinjiang Endemic and Ethnic Diseses, The First Affiliated Hospital, Shihezi University School of Medicine, Xinjiang, 832002, People's Republic of China. lifeng7855@126.com.
Shihezi University · CNBeijing Friendship Hospital · CNCapital Medical University · CN

Funding

National Natural Science Foundation of China 81460363National Natural Science Foundation of China 81560399National Natural Science Foundation of China 81760428National Natural Science Foundation of China 81773116
6 · The paper itself

Abstract

backgroundTumour-associated macrophages (TAMs) play an important role in the growth, progression, and metastasis of tumours. Epithelial-mesenchymal transition (EMT) is a mechanism for tumour invasion and metastasis. In this study, we aimed to determine whether TAMs can induce EMT for the invasion and metastasis of Kazakh oesophageal squamous cell cancer (ESCC).

methodsCD163 was used as a marker for TAMs, and the density of TAMs in tumour nest and surrounding stroma was quantified using immunohistochemistry (IHC). IHC staining was used to evaluate the expression of E-cadherin (epithelial marker) and vimentin (mesenchymal marker) in Kazakh ESCC and cancer-adjacent normal tissues (CANs). Additionally, 6-well transwell plates (0.4 μm) were used to establish the co-culture system of ESCC (EC109 or EC9706) cells and macrophages. Real-time quantitative polymerase chain reaction (qPCR) and western blot experiments were used to determine whether ESCC cells undergo EMT transformation after co-culture with macrophages. Transwell assays were used to detect the migration and invasion of the ESCC cells.

resultsThe distribution of CD163-positive TAMs in cancer tissues was closely related to EMT in Kazakh ESCC. The expression of vimentin in the ESCC cells was significantly upregulated, the expression of E-cadherin was significantly downregulated, and the invasion and migration of the ESCC cells were significantly enhanced after tumour-associated macrophages were added to the co-culture.

conclusionsTumour-associated macrophages promote EMT in ESCC, which may be one of the important factors involved in the invasion and progression of Kazakh ESCC.

Indexed as

Epithelial-Mesenchymal TransitionAdultAgedAntigens, CDAntigens, Differentiation, MyelomonocyticCadherinsCarcinoma, Transitional CellCD163 AntigenCell Line, TumorCell MovementEsophageal NeoplasmsEsophageal Squamous Cell CarcinomaFemaleHumansImmunohistochemistryMacrophagesAntigens, CDAntigens, Differentiation, MyelomonocyticCadherinsCD163 AntigenReceptors, Cell SurfaceEpithelial-mesenchymal transitionKazakhMigration and invasionOesophageal squamous cell carcinomaTumour-associated macrophages

Identifiers

PMID31186031
PMCPMC6560903
OpenAlexW2952799373

What OpenQuestion holds

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LicenceCC BY
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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.