Literature DB >> 31474359

Heterozygous Tumor Suppressor Microenvironment in Cancer Development.

Jean-Philippe Brosseau1, Lu Q Le2.   

Abstract

Hereditary cancer syndromes are typically caused by mutations of a tumor suppressor gene that lead to the early development of multifocal benign neoplasms followed by their malignant progression. However, the term 'hereditary cancer syndrome' may be misleading, as a large subgroup of syndromes are characterized by highly penetrant benign tumors. The reason why these cardinal tumors rarely progress to malignancy has been an elusive question in cancer biology. In this opinion article, we propose a framework where a heterozygous tumor suppressor gene microenvironment has antagonistic roles in tumorigenesis, by accelerating development of benign tumors while restraining further progression to malignant cancers.
Copyright © 2019 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  MPNST; NF1; STK11; benign tumor; hereditary benign tumor syndromes; hereditary cancer; malignant peripheral nerve sheath tumor; neurofibroma; tumor microenvironment; tumor suppressor gene

Year:  2019        PMID: 31474359      PMCID: PMC6724550          DOI: 10.1016/j.trecan.2019.07.004

Source DB:  PubMed          Journal:  Trends Cancer        ISSN: 2405-8025


  34 in total

1.  Concise handbook of familial cancer susceptibility syndromes - second edition.

Authors:  Noralane M Lindor; Mary L McMaster; Carl J Lindor; Mark H Greene
Journal:  J Natl Cancer Inst Monogr       Date:  2008

2.  Neurofibromas in NF1: Schwann cell origin and role of tumor environment.

Authors:  Yuan Zhu; Pritam Ghosh; Patrick Charnay; Dennis K Burns; Luis F Parada
Journal:  Science       Date:  2002-05-03       Impact factor: 47.728

3.  Neurofibromatosis-1 (Nf1) heterozygous brain microglia elaborate paracrine factors that promote Nf1-deficient astrocyte and glioma growth.

Authors:  Girish C Daginakatte; David H Gutmann
Journal:  Hum Mol Genet       Date:  2007-03-30       Impact factor: 6.150

4.  The neurofibromatosis type 1 (Nf1) tumor suppressor is a modifier of carcinogen-induced pigmentation and papilloma formation in C57BL/6 mice.

Authors:  R P Atit; K Mitchell; L Nguyen; D Warshawsky; N Ratner
Journal:  J Invest Dermatol       Date:  2000-06       Impact factor: 8.551

5.  Neurofibromatosis-1 heterozygosity increases microglia in a spatially and temporally restricted pattern relevant to mouse optic glioma formation and growth.

Authors:  Grant W Simmons; Winnie W Pong; Ryan J Emnett; Crystal R White; Scott M Gianino; Fausto J Rodriguez; David H Gutmann
Journal:  J Neuropathol Exp Neurol       Date:  2011-01       Impact factor: 3.685

6.  Malignant peripheral nerve sheath tumours in neurofibromatosis 1.

Authors:  D G R Evans; M E Baser; J McGaughran; S Sharif; E Howard; A Moran
Journal:  J Med Genet       Date:  2002-05       Impact factor: 6.318

7.  Loss of the Lkb1 tumour suppressor provokes intestinal polyposis but resistance to transformation.

Authors:  Nabeel Bardeesy; Manisha Sinha; Aram F Hezel; Sabina Signoretti; Nathaniel A Hathaway; Norman E Sharpless; Massimo Loda; Daniel R Carrasco; Ronald A DePinho
Journal:  Nature       Date:  2002-09-12       Impact factor: 49.962

8.  Multi-stage chemical carcinogenesis in mouse skin: fundamentals and applications.

Authors:  Erika L Abel; Joe M Angel; Kaoru Kiguchi; John DiGiovanni
Journal:  Nat Protoc       Date:  2009-08-27       Impact factor: 13.491

9.  Optic nerve glioma in mice requires astrocyte Nf1 gene inactivation and Nf1 brain heterozygosity.

Authors:  M Livia Bajenaru; M Rosario Hernandez; Arie Perry; Yuan Zhu; Luis F Parada; Joel R Garbow; David H Gutmann
Journal:  Cancer Res       Date:  2003-12-15       Impact factor: 12.701

10.  Are different events involved in the development of sporadic versus hereditary tumours? The possible importance of the microenvironment in hereditary cancer.

Authors:  C Paraskeva; A C Williams
Journal:  Br J Cancer       Date:  1990-06       Impact factor: 7.640

View more
  2 in total

1.  A Distinctive Adnexal (Usually Paratubal) Neoplasm Often Associated With Peutz-Jeghers Syndrome and Characterized by STK11 Alterations (STK11 Adnexal Tumor): A Report of 22 Cases.

Authors:  Jennifer A Bennett; Robert H Young; Brooke E Howitt; Sabrina Croce; Pankhuri Wanjari; Chaojie Zhen; Arnaud Da Cruz Paula; Emily Meserve; J Kenneth Schoolmeester; Sofia Westbom-Fremer; Eduardo Benzi; Ninad M Patil; Loes Kooreman; Mona El-Bahrawy; Gian Franco Zannoni; Thomas Krausz; W Glenn McCluggage; Britta Weigelt; Lauren L Ritterhouse; Esther Oliva
Journal:  Am J Surg Pathol       Date:  2021-08-01       Impact factor: 6.298

2.  Human cutaneous neurofibroma matrisome revealed by single-cell RNA sequencing.

Authors:  Jean-Philippe Brosseau; Adwait A Sathe; Yong Wang; Toan Nguyen; Donald A Glass; Chao Xing; Lu Q Le
Journal:  Acta Neuropathol Commun       Date:  2021-01-07       Impact factor: 7.801

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.