Literature DB >> 6588046

Random and nonrandom processes in metastasis, and metastatic inefficiency.

L Weiss.   

Abstract

Basically two hypotheses can be used to account for the metastatic inefficiency of cancer cells. The first is that the inefficiency is apparent, and reflects the small proportions of cells of a preexisting metastatic phenotype in primary tumors which are available for metastasis; thus, metastasis and metastatic inefficiency result from nonrandom processes. The opposed view is that most cancer cells have metastatic potential which is not realized unless they randomly enter a transient metastatic compartment which increases their chances of random survival in the metastatic cascade; thus, metastasis and metastatic inefficiency are basically random events. Discussion of this issue has been confused by the indisputable existence of cancer cell heterogeneity and cell lines with 'high' and 'low' metastatic or metastasis-related behavior. However, the relationship of these lines to naturally occurring metastasis is not at all clear. The evidence suggests that metastasis and metastatic inefficiency are determined by a series of random events, and although the presence of metastatic variants could alter the rate or efficiency with which metastasis occurs, they are not expected to determine whether they occur or not, or to produce major modifications in either.

Entities:  

Mesh:

Year:  1983        PMID: 6588046

Source DB:  PubMed          Journal:  Invasion Metastasis        ISSN: 0251-1789


  27 in total

Review 1.  The significance of biological heterogeneity.

Authors:  H Rubin
Journal:  Cancer Metastasis Rev       Date:  1990-07       Impact factor: 9.264

2.  Improving survival after large bowel cancer.

Authors:  T G Allen-Mersh
Journal:  BMJ       Date:  1991-09-14

3.  Comments on 'In vivo selection of human renal carcinoma cells with high metastatic potenital in nude mice'.

Authors:  L Weiss
Journal:  Clin Exp Metastasis       Date:  1990 Jan-Feb       Impact factor: 5.150

4.  Differential tumor growth of blood-borne B16 melanoma variants in cerebral dura mater is related to tumor-host cell reactions.

Authors:  T Kawaguchi; M Kawaguchi; T M Lembo; G L Nicolson
Journal:  Clin Exp Metastasis       Date:  1989 Jan-Feb       Impact factor: 5.150

5.  Dynamic heterogeneity: metastatic variants to liver are generated spontaneously in mouse embryonal carcinoma cells.

Authors:  J F Harris; M W Best
Journal:  Clin Exp Metastasis       Date:  1988 Nov-Dec       Impact factor: 5.150

Review 6.  Microvascular endothelial cell heterogeneity: interactions with leukocytes and tumor cells.

Authors:  P N Belloni; R J Tressler
Journal:  Cancer Metastasis Rev       Date:  1990-02       Impact factor: 9.264

Review 7.  Quantitative genetic analysis of tumor progression.

Authors:  V Ling; A F Chambers; J F Harris; R P Hill
Journal:  Cancer Metastasis Rev       Date:  1985       Impact factor: 9.264

8.  Differential organ tissue adhesion, invasion, and growth properties of metastatic rat mammary adenocarcinoma cells.

Authors:  G L Nicolson
Journal:  Breast Cancer Res Treat       Date:  1988-10       Impact factor: 4.872

Review 9.  Steps in tumor metastasis: new concepts from intravital videomicroscopy.

Authors:  A F Chambers; I C MacDonald; E E Schmidt; S Koop; V L Morris; R Khokha; A C Groom
Journal:  Cancer Metastasis Rev       Date:  1995-12       Impact factor: 9.264

10.  Dynamic heterogeneity: isolation of murine tumor cell populations enriched for metastatic variants and quantification of the unstable expression of the phenotype.

Authors:  S D Young; R P Hill
Journal:  Clin Exp Metastasis       Date:  1986 Jul-Sep       Impact factor: 5.150

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