Evidence map›Paper›PMID 36424360›Full record

ReviewCancer communications (London, England)2023

Signaling pathways in cancer-associated fibroblasts: recent advances and future perspectives.

Zengli Fang, Qingcai Meng, Jin Xu, Wei Wang, Bo Zhang, Jiang Liu, Chen Liang, Jie Hua, Yingjun Zhao, Xianjun Yu and 1 more

2 registry-linked trialsOpen access · goldAbstract readReview
In one paragraph

Review in Cancer communications (London, England), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 192 papers.

0numbers the graph read from it
0cells of the map it votes in
192citing papers in PubMed
18.7field-weighted citation impact, top 1% 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.

NCT01064622 phase2completednot on this map

A Multi-center, Double Blind, Placebo-Controlled, Randomized Phase II Trial of Gemcitabine Plus GDC-0449 (NSC 747691), a Hh Pathway Inhibitor, in Patients With Metastatic Pancreatic Cancer (10052747)

TypeinterventionalSponsorNational Cancer Institute (NCI)Ran2009 to 2013Enrolled118ConditionsPancreatic Adenocarcinoma, Recurrent Pancreatic Carcinoma, Stage IV Pancreatic Cancer AJCC v6 and v7ArmsGemcitabine Hydrochloride, Hydrocortisone/Placebo, Vismodegib
NCT01130142 phase1 / phase2completednot on this map

A Phase 1b/2 Study Evaluating IPI-926 in Combination With Gemcitabine in Patients With Metastatic Pancreatic Cancer

TypeinterventionalSponsorInfinity Pharmaceuticals, Inc.Ran2010 to 2012Enrolled122ConditionsMetastatic Pancreatic CancerArmsIPI-926 plus gemcitabine, Placebo plus gemcitabine
3 · Its place in the literature

Who cites it

192 citing papers in PubMed, 243 citations in OpenAlex.

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  18. Cytokines and cancer-associated fibroblasts.Journal of hematology & oncology · 2026
    Review
  19. Review
  20. Article

132 more citing papers are in PubMed but not listed here.

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.

Zengli FangDepartment of Pancreatic Surgery, Fudan University Shanghai Cancer Center, Shanghai, 200032, P. R. China.
Qingcai MengDepartment of Pancreatic Surgery, Fudan University Shanghai Cancer Center, Shanghai, 200032, P. R. China.
Jin XuDepartment of Pancreatic Surgery, Fudan University Shanghai Cancer Center, Shanghai, 200032, P. R. China.
Wei WangDepartment of Pancreatic Surgery, Fudan University Shanghai Cancer Center, Shanghai, 200032, P. R. China.
Bo ZhangDepartment of Pancreatic Surgery, Fudan University Shanghai Cancer Center, Shanghai, 200032, P. R. China.
Jiang LiuDepartment of Pancreatic Surgery, Fudan University Shanghai Cancer Center, Shanghai, 200032, P. R. China.
Chen LiangDepartment of Pancreatic Surgery, Fudan University Shanghai Cancer Center, Shanghai, 200032, P. R. China.
Jie HuaDepartment of Pancreatic Surgery, Fudan University Shanghai Cancer Center, Shanghai, 200032, P. R. China.
Yingjun ZhaoDepartment of Oncology, Shanghai Medical College, Fudan University, Shanghai, 200032, P. R. China.
Xianjun YuDepartment of Pancreatic Surgery, Fudan University Shanghai Cancer Center, Shanghai, 200032, P. R. China.ORCID https://orcid.org/0000-0002-6697-7143
Si ShiDepartment of Pancreatic Surgery, Fudan University Shanghai Cancer Center, Shanghai, 200032, P. R. China.ORCID https://orcid.org/0000-0002-6652-0629
Shanghai Medical College of Fudan University · CN

Funding

Clinical and Scientific Innovation Project of Shanghai Hospital Development Center SHDC12018109Clinical and Scientific Innovation Project of Shanghai Hospital Development Center SHDC12019109National Natural Science Foundation of China 81772555National Natural Science Foundation of China 81802352National Natural Science Foundation of China 81902428National Natural Science Foundation of China 82002541National Science Foundation for Distinguished Young Scholars of China 81625016Scientific Innovation Project of Shanghai Education Committee 2019-01-07-00-07-E00057Shanghai Anticancer Association Young Eagle Program SACA-CY19A06Shanghai Rising-Star Program 20QA1402100Shanghai Sailing Program 20YF1409000
6 · The paper itself

Abstract

As a critical component of the tumor microenvironment (TME), cancer-associated fibroblasts (CAFs) play important roles in cancer initiation and progression. Well-known signaling pathways, including the transforming growth factor-β (TGF-β), Hedgehog (Hh), Notch, Wnt, Hippo, nuclear factor kappa-B (NF-κB), Janus kinase (JAK)/signal transducer and activator of transcription (STAT), mitogen-activated protein kinase (MAPK), and phosphoinositide 3-kinase (PI3K)/AKT pathways, as well as transcription factors, including hypoxia-inducible factor (HIF), heat shock transcription factor 1 (HSF1), P53, Snail, and Twist, constitute complex regulatory networks in the TME to modulate the formation, activation, heterogeneity, metabolic characteristics and malignant phenotype of CAFs. Activated CAFs remodel the TME and influence the malignant biological processes of cancer cells by altering the transcriptional and secretory characteristics, and this modulation partially depends on the regulation of signaling cascades. The results of preclinical and clinical trials indicated that therapies targeting signaling pathways in CAFs demonstrated promising efficacy but were also accompanied by some failures (e.g., NCT01130142 and NCT01064622). Hence, a comprehensive understanding of the signaling cascades in CAFs might help us better understand the roles of CAFs and the TME in cancer progression and may facilitate the development of more efficient and safer stroma-targeted cancer therapies. Here, we review recent advances in studies of signaling pathways in CAFs and briefly discuss some future perspectives on CAF research.

Indexed as

Cancer-Associated FibroblastsNeoplasmsHedgehog ProteinsHumansNF-kappa BPhosphatidylinositol 3-KinasesSignal TransductionTumor MicroenvironmentHedgehog ProteinsNF-kappa BPhosphatidylinositol 3-KinasesCancer-associated fibroblastsCell-cell interactionSignaling pathwaysTherapeutic targetsTumor microenvironment

Identifiers

PMID36424360
PMCPMC9859735
OpenAlexW4310079132

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

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.