Evidence map›Paper›PMID 33454798›Full record

ArticleCancer immunology, immunotherapy : CII2021

Dopamine improves chemotherapeutic efficacy for pancreatic cancer by regulating macrophage-derived inflammations.

Qiaofei Liu, Ronghua Zhang, Xiang Zhang, Jingkai Liu, Huanwen Wu, Yuan Li, Ming Cui, Tong Li, Huixin Song, Junyi Gao and 3 more

Open access · greenAbstract read
In one paragraph

Article in Cancer immunology, immunotherapy : CII, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

24 citing papers in PubMed, 31 citations in OpenAlex.

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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

13 authors at 2 institutions in 1 country.

Qiaofei Liu *Department of General Surgery, Peking Union Medical College and Chinese Academy of Medical Sciences, Peking Union Medical College Hospital, 1# Shuai Fu Yuan, Dongcheng District, Beijing, 100730, China.ORCID http://orcid.org/0000-0001-9889-2833
Ronghua Zhang *Department of General Surgery, Peking Union Medical College and Chinese Academy of Medical Sciences, Peking Union Medical College Hospital, 1# Shuai Fu Yuan, Dongcheng District, Beijing, 100730, China.
Xiang Zhang *Department of General Surgery, Peking Union Medical College and Chinese Academy of Medical Sciences, Peking Union Medical College Hospital, 1# Shuai Fu Yuan, Dongcheng District, Beijing, 100730, China.
Jingkai LiuDepartment of General Surgery, Peking Union Medical College and Chinese Academy of Medical Sciences, Peking Union Medical College Hospital, 1# Shuai Fu Yuan, Dongcheng District, Beijing, 100730, China.
Huanwen WuDepartment of Pathology, Peking Union Medical College and Chinese Academy of Medical Sciences, Peking Union Medical College Hospital, Beijing, 100730, China.
Yuan LiDepartment of Pathology, Peking Union Medical College and Chinese Academy of Medical Sciences, Peking Union Medical College Hospital, Beijing, 100730, China.
Ming CuiDepartment of General Surgery, Peking Union Medical College and Chinese Academy of Medical Sciences, Peking Union Medical College Hospital, 1# Shuai Fu Yuan, Dongcheng District, Beijing, 100730, China.
Tong LiDepartment of General Surgery, Peking Union Medical College and Chinese Academy of Medical Sciences, Peking Union Medical College Hospital, 1# Shuai Fu Yuan, Dongcheng District, Beijing, 100730, China.
Huixin SongDepartment of General Surgery, Peking Union Medical College and Chinese Academy of Medical Sciences, Peking Union Medical College Hospital, 1# Shuai Fu Yuan, Dongcheng District, Beijing, 100730, China.
Junyi GaoDepartment of General Surgery, Peking Union Medical College and Chinese Academy of Medical Sciences, Peking Union Medical College Hospital, 1# Shuai Fu Yuan, Dongcheng District, Beijing, 100730, China.
Yalu ZhangDepartment of General Surgery, Peking Union Medical College and Chinese Academy of Medical Sciences, Peking Union Medical College Hospital, 1# Shuai Fu Yuan, Dongcheng District, Beijing, 100730, China.
Sen YangDepartment of General Surgery, Peking Union Medical College and Chinese Academy of Medical Sciences, Peking Union Medical College Hospital, 1# Shuai Fu Yuan, Dongcheng District, Beijing, 100730, China.
Quan LiaoDepartment of General Surgery, Peking Union Medical College and Chinese Academy of Medical Sciences, Peking Union Medical College Hospital, 1# Shuai Fu Yuan, Dongcheng District, Beijing, 100730, China. lqpumc@126.com.
Chinese Academy of Medical Sciences & Peking Union Medical College · CNShandong University · CN

Funding

Beijing Natural Science Foundation of China 7172177National Natural Science Foundation of China 81673023National Natural Science Foundation of China 81872501National Science and Technology Planning Project (CN) 81502068
6 · The paper itself

Abstract

Pancreatic cancer is an inflammatory malignancy, and tumor-associated macrophages (TAMs) are the predominant inflammatory cells in tumor tissue. TAMs have complicated interactions with pancreatic cancer cells, however, the details and mechanisms remain largely unknown. In this study, transcriptomics and proteomics analyses were performed to explore the interactions between murine pancreatic cancer cells and TAMs. Dopamine (DA) has been reported to suppress inflammations. However, its roles in TAMs of pancreatic cancer have not been reported. Herein, the roles and mechanisms of DA to affect the chemotherapeutic efficacy for pancreatic cancer were studied. Multi-omics results revealed that there was a tumor-promoting vicious cycle involving murine pancreatic cancer cells and TAMs. DA substantially improved the chemotherapeutic efficacy both in vitro study and in immunocompetent murine pancreatic cancer models by suppression of the M2 characters of TAMs. Further studies found that activation of DRD4 by DA led to the decrease of cAMP, and then inhibited the activation of PKA/p38 signal pathway, which suppressed the tumor-promoting inflammation of TAMs. This study uncovers the reciprocal interactions between TAMs and pancreatic cancer cells using multi-omics techniques and presents that DA has synergistic roles with chemotherapy for pancreatic cancer by suppressing of TAM-derived inflammations.

Indexed as

AnimalsCell LineCell Line, TumorDopamineInflammationMacrophagesMaleMiceMice, Inbred C57BLPancreatic NeoplasmsRAW 264.7 CellsReceptors, Dopamine D4Signal TransductionTumor MicroenvironmentDopamineReceptors, Dopamine D4ChemotherapyDopamineMulti-omics analysisPancreatic cancerTumor-associated macrophages

Identifiers

PMID33454798
PMCPMC10991349
OpenAlexW3125669801

What OpenQuestion holds

Textmetadata
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.