Evidence map›Paper›PMID 22124844›Full record

ReviewHormones & cancer2012

Mechanisms of HGF/Met signaling to Brk and Sam68 in breast cancer progression.

Alessia Locatelli, Kristopher A Lofgren, Andrea R Daniel, Nancy E Castro, Carol A Lange

Open access · bronzeAbstract readReview
In one paragraph

Review in Hormones & cancer, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing 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

31 citing papers in PubMed, 55 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Targeting protein tyrosine kinase 6 in cancer.Biochimica et biophysica acta. Reviews on cancer · 2020
    Review
  8. CREB5 promotes invasiveness and metastasis in colorectal cancer by directly activating MET.Journal of experimental & clinical cancer research : CR · 2020
    Article
  9. Protein tyrosine kinase 6 signaling in prostate cancer.American journal of clinical and experimental urology · 2020
    Review
  10. Article
  11. Review
  12. Review
  13. Article
  14. Sam68 is Overexpressed in Epithelial Ovarian Cancer and Promotes Tumor Cell Proliferation.Medical science monitor : international medical journal of experimental and clinical research · 2016
    Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. Article
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

5 authors at 1 institution in 1 country.

Alessia LocatelliDepartment of Medicine, Division of Hematology, Oncology and Transplantation, University of Minnesota, Minneapolis, 55455, USA.
Kristopher A Lofgren
Andrea R Daniel
Nancy E Castro
Carol A Lange
University of Minnesota · US

Funding

TRAINING GRANT IN MICROBIOLOGY/CANCER RESEARCHT32CA009138 · NCI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI Scott M. Dehm · 1985 to 2026
$11.3M
Brk signal transduction in breast cancerR01CA107547 · NCI · UNIVERSITY OF MINNESOTA · PI LANGE, CAROL A · 2007 to 2011
$1.3M
NCI NIH HHS CA107547NCI NIH HHS R01 CA107547NCI NIH HHS T32 CA009138
6 · The paper itself

Abstract

Signal transduction pathways downstream of receptor tyrosine kinases (RTKs) are often deregulated during oncogenesis, tumor progression, and metastasis. In particular, the peptide growth factor hormone, hepatocyte growth factor (HGF), and its specific receptor, Met tyrosine kinase, regulate cancer cell migration, thereby conferring an aggressive phenotype (Nakamura et al., J Clin Invest 106(12):1511-1519, 2000; Huh et al., Proc Natl Acad Sci U S A 101:4477-4482, 2004). Additionally, overexpression of Met is associated with enhanced invasiveness of breast cancer cells (Edakuni et al., Pathol Int 51(3):172-178, 2001; Jin et al., Cancer 79(4):749-760, 1997; Tuck et al., Am J Pathol 148(1):225-232, 1996). Here, we review the regulation of recently identified novel downstream mediators of HGF/Met signaling, Breast tumor kinase (Brk/PTK6), and Src-associated substrate during mitosis of 68 kDa (Sam68), and discuss their relevance to mechanisms of breast cancer progression.

Indexed as

Adaptor Proteins, Signal TransducingBreastBreast NeoplasmsCell MovementDisease ProgressionDNA-Binding ProteinsFemaleHepatocyte Growth FactorHumansMitogen-Activated Protein Kinase 7Neoplasm ProteinsPhosphorylationProtein Structure, TertiaryProtein-Tyrosine KinasesProto-Oncogene Proteins c-metRNA-Binding ProteinsAdaptor Proteins, Signal TransducingDNA-Binding ProteinsHepatocyte Growth FactorHGF protein, humanKHDRBS1 protein, humanMET protein, humanMitogen-Activated Protein Kinase 7Neoplasm ProteinsProtein-Tyrosine KinasesProto-Oncogene Proteins c-metPTK6 protein, humanRNA-Binding ProteinsTyrosine

Identifiers

PMID22124844
PMCPMC3971994
OpenAlexW2006344933

What OpenQuestion holds

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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.