Evidence map›Paper›PMID 39186144›Full record

ReviewDiscover oncology2024

The complex role of macrophages in pancreatic cancer tumor microenvironment: a review on cancer progression and potential therapeutic targets.

Parsa Lorestani, Mohsen Dashti, Negar Nejati, Mohammad Amin Habibi, Mandana Askari, Behruz Robat-Jazi, Sajjad Ahmadpour, Soheil Tavakolpour

Abstract readReview
In one paragraph

Review in Discover oncology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Review
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  3. Article
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  5. Article
  6. Review
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  10. Article
  11. Review
  12. Review
  13. Updates in Immunotherapy for Pancreatic Cancer.Journal of clinical medicine · 2024
    Review
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

8 authors.

Parsa Lorestani *Students Research Committee, Kermanshah University of Medical Sciences, Kermanshah, Iran.ORCID http://orcid.org/0009-0008-7217-3097
Mohsen Dashti *Immunology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.ORCID http://orcid.org/0000-0003-4455-7858
Negar NejatiPediatric Cell and Gene Therapy Research Centre, Gene, Cell & Tissue Research Institute, Tehran University of Medical Sciences, Tehran, Iran.ORCID http://orcid.org/0000-0002-8192-8542
Mohammad Amin HabibiDepartment of Neurosurgery, Shariati Hospital, Tehran University of Medical Sciences, Tehran, Iran.ORCID http://orcid.org/0000-0001-7600-6925
Mandana AskariDepartment of Nanobiotechnology, Faculty of Biological Sciences, Tarbiat Modares University, Tehran, Iran.ORCID http://orcid.org/0000-0003-3903-7049
Behruz Robat-JaziDepartment of Immunology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran.ORCID http://orcid.org/0000-0001-7366-0972
Sajjad AhmadpourPatient Safety Research Center, Clinical Research Institute, Urmia University of Medical Sciences, Urmia, Iran. sajjadahmadpour@yahoo.com.ORCID http://orcid.org/0000-0003-4321-874X
Soheil TavakolpourDana-Farber Cancer Institute, Harvard Medical School, Boston, MA, 02215, USA. soheil_tavakolpour@dfci.harvard.edu.ORCID http://orcid.org/0000-0002-6765-8830

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pancreatic cancer (PC) is one of the deadliest cancers worldwide with low survival rates and poor outcomes. The treatment landscape for PC is fraught with obstacles, including drug resistance, lack of effective targeted therapies and the immunosuppressive tumor microenvironment (TME). The resistance of PC to existing immunotherapies highlights the need for innovative approaches, with the TME emerging as a promising therapeutic target. The recent advancements in understanding the role of macrophages, this context highlight their significant impact on tumor development and progression. There are two important types of macrophages: M1 and M2, which play critical roles in the TME. Therapeutics strategies including, depletion of tumor-associated macrophages (TAMs), reprogramming TAMs to promote anti-tumor activity, and targeting macrophage recruitment can lead to promising outcomes. Targeting macrophage-related pathways may offer novel strategies for modulating immune responses, inhibiting angiogenesis, and overcoming resistance to chemotherapy in PC treatment.

Indexed as

ImmunotherapiesMacrophagesMacrophage-targeted therapyPancreatic cancerPancreatic ductal adenocarcinomaTumor microenvironment

Identifiers

PMID39186144
PMCPMC11347554

What OpenQuestion holds

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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.