↓ Skip to main content

Proteases and Cancer

Overview of attention for book
Cover of 'Proteases and Cancer'

Table of Contents

  1. Altmetric Badge
    Book Overview
  2. Altmetric Badge
    Chapter 1 Dissecting Degradomes: Analysis of Protease-Coding Genes
  3. Altmetric Badge
    Chapter 2 Identification of Protease Cleavage Sites and Substrates in Cancer by Carboxy-TAILS (C-TAILS)
  4. Altmetric Badge
    Chapter 3 Identification of Proteolytic Cleavage Sites of EphA2 by Membrane Type 1 Matrix Metalloproteinase on the Surface of Cancer Cells
  5. Altmetric Badge
    Chapter 4 Biotin-Chasing Assay to Evaluate uPAR Stability and Cleavage on the Surface of Cells
  6. Altmetric Badge
    Chapter 5 Determination of Aconitase Activity: A Substrate of the Mitochondrial Lon Protease
  7. Altmetric Badge
    Chapter 6 A Simple Cell-Based Assay for the Detection of Surface Protein Shedding by Rhomboid Proteases
  8. Altmetric Badge
    Chapter 7 Functional Production of Catalytic Domains of Human MMPs in Escherichia coli Periplasm
  9. Altmetric Badge
    Chapter 8 Autophagy and Proteases: Basic Study of the Autophagic Flux by Western Blot
  10. Altmetric Badge
    Chapter 9 Gel-Based Gelatin Zymography to Examine Matrix Metalloproteinase Activity in Cell Culture
  11. Altmetric Badge
    Chapter 10 Analysis of Enzymatic Activity of Matrix Metalloproteinase (MMP) by Collagen Zymography in Melanoma
  12. Altmetric Badge
    Chapter 11 Measurement of Protease Activities Using Fluorogenic Substrates
  13. Altmetric Badge
    Chapter 12 Targeting the Expression of Cathepsin B Using CRISPR/Cas9 System in Mammalian Cancer Cells
  14. Altmetric Badge
    Chapter 13 Assessing the Influence of a Protease in Cell Migration Using the Barrier-Migration Assay
  15. Altmetric Badge
    Chapter 14 Analysis of Invasive Activity of CAF Spheroids into Three Dimensional (3D) Collagen Matrices
  16. Altmetric Badge
    Chapter 15 Beyond the Proteolytic Activity: Examining the Functional Relevance of the Ancillary Domains Using Tri-Dimensional (3D) Spheroid Invasion Assay
  17. Altmetric Badge
    Chapter 16 Analyzing the Type II Transmembrane Serine Protease Hepsin-Dependent Basement Membrane Remodeling in 3D Cell Culture
  18. Altmetric Badge
    Chapter 17 Evaluation of Tumor Vasculature Using a Syngeneic Tumor Model in Wild-Type and Genetically Modified Mice
  19. Altmetric Badge
    Chapter 18 3D Image Analysis of the Microvasculature in Healthy and Diseased Tissues
  20. Altmetric Badge
    Chapter 19 Human Tumor Tissue-Based 3D In Vitro Invasion Assays
  21. Altmetric Badge
    Chapter 20 Ear Sponge Assay: A Method to Investigate Angiogenesis and Lymphangiogenesis in Mice
  22. Altmetric Badge
    Chapter 21 Cancer Susceptibility Models in Protease-Deficient Mice
  23. Altmetric Badge
    Chapter 22 Imaging Proteolytic Activities in Mouse Models of Cancer
  24. Altmetric Badge
    Chapter 23 Protease Silencing to Explore the Molecular Mechanisms of Cancer and Aging
  25. Altmetric Badge
    Chapter 24 Analysis of Somatic DNA Methylation Alterations of Genes Encoding Cell Surface Metallopeptidases in Colorectal Cancer
  26. Altmetric Badge
    Chapter 25 Targeting Deubiquitinases in Cancer
  27. Altmetric Badge
    Chapter 26 Generation of Highly Selective MMP Antibody Inhibitors
  28. Altmetric Badge
    Chapter 27 Strategies to Target Matrix Metalloproteinases as Therapeutic Approach in Cancer
Attention for Chapter 2: Identification of Protease Cleavage Sites and Substrates in Cancer by Carboxy-TAILS (C-TAILS)
Altmetric Badge

About this Attention Score

  • Average Attention Score compared to outputs of the same age and source

Mentioned by

twitter
2 X users

Readers on

mendeley
6 Mendeley
You are seeing a free-to-access but limited selection of the activity Altmetric has collected about this research output. Click here to find out more.
Chapter title
Identification of Protease Cleavage Sites and Substrates in Cancer by Carboxy-TAILS (C-TAILS)
Chapter number 2
Book title
Proteases and Cancer
Published in
Methods in molecular biology, January 2018
DOI 10.1007/978-1-4939-7595-2_2
Pubmed ID
Book ISBNs
978-1-4939-7594-5, 978-1-4939-7595-2
Authors

Nestor Solis, Christopher M. Overall

Abstract

Determination of drug targets and development of novel therapeutics for the treatment of different cancers are actively ongoing areas of research. Proteases being the second largest group of enzymes in humans present themselves as attractive targets for blocking and activation to treat malignancies. However, determination of the protease cleavage substrates is often missed by utilizing conventional modern proteomic approaches. The relatively low abundance of proteolytically processed, and mostly semi-tryptic, peptides compared to tryptic peptides generated in shotgun proteomics compounded with their poorer identification rates makes the identification of such critical peptides challenging and so are mostly overlooked. Our laboratory introduced Terminal Amine Isotopic Labeling of Substrates (TAILS) to identify N-terminal peptides from cleavage events. In this chapter we present a protocol from our complementary method carboxy-TAILS (C-TAILS) to identify C-terminal peptides in metabolically labeled cancer cell lines.

X Demographics

X Demographics

The data shown below were collected from the profiles of 2 X users who shared this research output. Click here to find out more about how the information was compiled.
Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 6 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 6 100%

Demographic breakdown

Readers by professional status Count As %
Unspecified 1 17%
Professor 1 17%
Student > Ph. D. Student 1 17%
Researcher 1 17%
Student > Master 1 17%
Other 0 0%
Unknown 1 17%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 4 67%
Unspecified 1 17%
Unknown 1 17%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 1. This is our high-level measure of the quality and quantity of online attention that it has received. This Attention Score, as well as the ranking and number of research outputs shown below, was calculated when the research output was last mentioned on 30 January 2019.
All research outputs
#17,925,346
of 23,015,156 outputs
Outputs from Methods in molecular biology
#7,288
of 13,165 outputs
Outputs of similar age
#310,377
of 442,344 outputs
Outputs of similar age from Methods in molecular biology
#868
of 1,498 outputs
Altmetric has tracked 23,015,156 research outputs across all sources so far. This one is in the 19th percentile – i.e., 19% of other outputs scored the same or lower than it.
So far Altmetric has tracked 13,165 research outputs from this source. They receive a mean Attention Score of 3.4. This one is in the 39th percentile – i.e., 39% of its peers scored the same or lower than it.
Older research outputs will score higher simply because they've had more time to accumulate mentions. To account for age we can compare this Altmetric Attention Score to the 442,344 tracked outputs that were published within six weeks on either side of this one in any source. This one is in the 25th percentile – i.e., 25% of its contemporaries scored the same or lower than it.
We're also able to compare this research output to 1,498 others from the same source and published within six weeks on either side of this one. This one is in the 36th percentile – i.e., 36% of its contemporaries scored the same or lower than it.