Ki-67 is an excellent marker to determine the growth fraction of a given cell population. The fraction of Ki-67-positive
tumor cells (the
Ki-67 labeling index) is often correlated with the clinical course of
cancer. The best-studied examples in this context are
prostate, brain and
breast carcinomas, as well as
nephroblastoma and
neuroendocrine tumors. For these types of tumors, the prognostic value for survival and tumor recurrence have repeatedly been proven in uni- and multivariate analysis.
MIB-1 Ki-67 and MIB-1 monoclonal antibodies are directed against different epitopes of the same proliferation-related antigen. Ki-67 and MIB-1 may be used on fixed sections. MIB-1 is used in clinical applications to determine the
Ki-67 labelling index. One of its primary advantages over the original Ki-67 antibody (and the reason why it has essentially supplanted the original antibody for clinical use) is that it can be used on formalin-fixed paraffin-embedded sections, after heat-mediated antigen retrieval (see next section below). File:Positive immunohistochemistry of KI-67 in invasive breast cancer.jpg|High Ki-67 expression in an invasive
breast cancer, with cancer nuclei being stained (brown). There is tumor cell positivity in 70% of the cells:
Ki-67 labelling index = 70% File:Counting Ki-67 index in immunohistochemistry.jpg|Counting positive versus negative nuclei with Ki-67 labeling, in this case in a neuroendocrine tumor of the small intestine. To count as positive, a nucleus should be at least half within the field of view, be large enough, and not be located in the stroma. Otherwise, even weakly positive nuclei count as positive.
Original Ki-67 antibody The Ki-67 protein was originally defined by the prototype monoclonal
antibody Ki-67, which was generated by immunizing mice with nuclei of the
Hodgkin lymphoma cell line L428. The name is derived from the city of origin (
Kiel, Germany) and the number of the original clone in the 96-well plate. == Interactions ==