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Defining precancer: a grand challenge for the cancer community

  • Jessica Faupel-Badger,
  • Indu Kohaar,
  • Manisha Bahl,
  • Andrew T. Chan,
  • Joshua D. Campbell,
  • Li Ding,
  • Angelo M. De Marzo,
  • Anirban Maitra,
  • Daniel T. Merrick,
  • Ernest T. Hawk,
  • Ignacio I. Wistuba,
  • Irene M. Ghobrial,
  • Scott M. Lippman,
  • Karen H. Lu,
  • Mark Lawler,
  • Neil E. Kay,
  • Thea D. Tlsty,
  • Timothy R. Rebbeck,
  • Sudhir Srivastava

摘要

The term ‘precancer’ typically refers to an early stage of neoplastic development that is distinguishable from normal tissue owing to molecular and phenotypic alterations, resulting in abnormal cells that are at least partially self-sustaining and function outside of normal cellular cues that constrain cell proliferation and survival. Although such cells are often histologically distinct from both the corresponding normal and invasive cancer cells of the same tissue origin, defining precancer remains a challenge for both the research and clinical communities. Once sufficient molecular and phenotypic changes have occurred in the precancer, the tissue is identified as a ‘cancer’ by a histopathologist. While even diagnosing cancer can at times be challenging, the determination of invasive cancer is generally less ambiguous and suggests a high likelihood of and potential for metastatic disease. The ‘hallmarks of cancer’ set out the fundamental organizing principles of malignant transformation but exactly how many of these hallmarks and in what configuration they define precancer has not been clearly and consistently determined. In this Expert Recommendation, we provide a starting point for a conceptual framework for defining precancer, which is based on molecular, pathological, clinical and epidemiological criteria, with the goal of advancing our understanding of the initial changes that occur and opportunities to intervene at the earliest possible time point.