Literature DB >> 6203864

Different metastatic potential of in vitro and in vivo lines selected from Lewis lung carcinoma: correlation with response to different bleomycin schedulings.

A Sacchi, F Calabresi, C Greco, G Zupi.   

Abstract

In vitro and in vivo variant cell lines selected from Lewis lung carcinoma are described. In vitro tumor lines are shown to differ in their metastatic potential, evaluated as lung colony-forming ability. Moreover, corresponding in vivo sublines, derived from intramuscular implant of cultured tumor cells, exhibit the same behavior for metastases formation as their in vitro counterpart. The metastatic potential of the in vivo lines has been evaluated both as lung colony-forming ability and as spontaneous metastasis formation. Response to bleomycin (BLM) treatment has been studied on the in vitro and the in vivo lines. Results reported show that the most metastatic lines, in vitro and in vivo, appear to be more resistant to a BLM treatment and that appropriate fractionation regimens can improve both the percentage of cell kill and the percentage of metastases reduction.

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Year:  1981        PMID: 6203864

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


  6 in total

1.  Wild-type p53 differentially affects tumorigenic and metastatic potential of murine metastatic cell variants.

Authors:  M G Rizzo; S Soddu; G Tibursi; B Calabretta; A Sacchi
Journal:  Clin Exp Metastasis       Date:  1993-09       Impact factor: 5.150

2.  Tumor heterogeneity: biological implications and therapeutic consequences.

Authors:  G H Heppner; B E Miller
Journal:  Cancer Metastasis Rev       Date:  1983       Impact factor: 9.264

3.  Changes of phenotypic characteristics of variants derived from Lewis lung carcinoma during long-term in vitro growth.

Authors:  A Sacchi; F Mauro; G Zupi
Journal:  Clin Exp Metastasis       Date:  1984 Apr-Jun       Impact factor: 5.150

4.  Metastatic dissemination of 3LL variants after treatment with monoclonal antibody to a tumor-associated antigen.

Authors:  A Sacchi; S Kennel; P G Natali; G Tibursi; C A Ghetti
Journal:  Clin Exp Metastasis       Date:  1987-09       Impact factor: 5.150

5.  Retinoic acid negatively regulates beta 4 integrin expression and suppresses the malignant phenotype in a Lewis lung carcinoma cell line.

Authors:  C Gaetano; A Melchiori; A Albini; R Benelli; R Falcioni; A Modesti; A Modica; S Scarpa; A Sacchi
Journal:  Clin Exp Metastasis       Date:  1994-01       Impact factor: 5.150

6.  Heterogeneity of circulating tumor cell dissemination and lung metastases in a subcutaneous Lewis lung carcinoma model.

Authors:  Jessica E Fitzgerald; Brook K Byrd; Roshani A Patil; Rendall R Strawbridge; Scott C Davis; Chiara Bellini; Mark Niedre
Journal:  Biomed Opt Express       Date:  2020-06-08       Impact factor: 3.732

  6 in total

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