Special Feature

User Panel

My Panel

My Panel

Bookmark Science Articles

Recent News
Bookmark / Share This Science Site

Tumor immunoediting and immunosculpting pathways to cancer progression.

Tumor immunoediting and immunosculpting pathways to cancer progression. Research Abstract Details 

Research Abstract Table of Contents

Jump to the:

  • Abstract Text of This Paper
  • Journal Published
  • MeSH Keywords of This Abstract
  • Chemicals and Substances Used in this Paper
  • Grants and Granting Agency of this Research
  • Database Accession Numbers Used in this Paper
  • Related Papers
  • Related Research Tags
  • Rate this Research Paper
  • Tumor immunoediting and immunosculpting pathways to cancer progression. Abstract Text:

    jennifer m reimanJennifer M Reiman,maciej kmieciakMaciej Kmieciak,masoud h manjiliMasoud H Manjili,keith l knutsonKeith L Knutson,

    Recent studies have suggested that a natural function of the immune system is to respond and destroy aberrant, dysfunctional cells by a process called immunosurveillance. These studies also suggest that the tumors that arise despite immunosurveillance have been immunosculpted by the immune system. The purported abilities of tumors to induce immune tolerance and suppression, the increased pathogenic behavior of the tumor cells following exposure to immune effectors and the loss of immunogenicity (i.e. immunoediting) often observed in advanced stage tumors could be the result of immunosculpting. In some cases, these immunosculpting features may be permanent and irreversible. However, in other cases, reversible epigenetic mechanisms may underlie the immune resistant tumor phenotype. Regardless, these immune-induced alterations could contribute to cancer pathogenesis. Understanding the mechanisms by which tumors evade immunity will be important for disease prevention and therapeutics.

    Tumor immunoediting and immunosculpting pathways to cancer progression. Publishing Authors By Initials

    jm reimanJM Reiman,m kmieciakM Kmieciak,mh manjiliMH Manjili,kl knutsonKL Knutson,

    For similar biological phenomena, cell phenomena, and immunity: immunity: tumor escape research abstracts see: biological phenomena, cell phenomena, and immunity: immunity: tumor escape research

    PUBMED ID PMID:

    MEDLINE DATE:

    Tumor immunoediting and immunosculpting pathways to cancer progression. Journal Published:

    PUBLICATION TYPE: Review

    Journal: Seminars in cancer biology

    VOLUME: 17

    Page Numbers: 275-87

    Journal Abbreviation: Semin. Cancer Biol.

    ISSN: 1044-579X

    DAY: 26

    MONTH: 06

    YEAR: 2007

    Tumor immunoediting and immunosculpting pathways to cancer progression. Information

    Number of References: 150

    LANGUAGE: eng

    NlmUniqueID: 9010218

    Tumor immunoediting and immunosculpting pathways to cancer progression. Keywords Mesh Terms:

    KEYWORDS: Tumor Escape

    MESH TERMS: immunology

    Chemical & Substance for Abstract: Tumor immunoediting and immunosculpting pathways to cancer progression. Information

    Substance Name: Antigens, Neoplasm

    Registry Number: 0

    Grant and Affiliation Information for Tumor immunoediting and immunosculpting pathways to cancer progression.

    AFFILIATION: Department of Immunology, Mayo Clinic College of Medicine, 200 First Street SW, Rochester, MN 55905, United States.

    Country: England

    England Research PublicationEngland Research Publication

    AGENCY: United States NCI

    GRANT: R01-CA113861

    ACRONYM: CA

    MEDLINETA: Semin Cancer Biol

    REFSOURCE:

    DATABASENAME:

    ACCESSION NUMBER:

    Number Hits: 0

    Tumor immunoediting and immunosculpting pathways to cancer progression Related Publications

     

    Molecular Station USER Menu

    Welcome to Molecular Station!

    You have to register before you can post on our forums or use our advanced features. Register Now! Its Free and Fast!

    Already registered? Login now below.

    User Name:

    Password:

    Already registered and Forgot your password? Click below to recover it.

    Recover Lost Password

    Join now - it's fast and free!

    Molecular Station is THE largest network of researchers, scientists and science lovers anywhere!

    Research Terms of Usage and Disclaimer
    Home
    Features

    Protocols

    DNA Forum

    Science Forum

    DNA Forum
    Biology Forum

    Science News


    [CaRP] XML error: Invalid document end at line 2

    For more click here:Science News