Squamous morules are functionally inert elements of premalignant endometrial neoplasia.

TitleSquamous morules are functionally inert elements of premalignant endometrial neoplasia.
Publication TypeJournal Article
Year of Publication2009
AuthorsLin M-C, Lomo L, Baak JPA, Eng C, Ince TA, Crum CP, Mutter GL
JournalMod Pathol
Volume22
Issue2
Pagination167-74
Date Published2009 Feb
ISSN1530-0285
KeywordsAdenocarcinoma, Biopsy, Carcinoma in Situ, Cell Proliferation, Cell Transformation, Neoplastic, DNA Mutational Analysis, Endometrial Neoplasms, Endometrium, Female, Gene Expression Regulation, Neoplastic, Humans, Hyperplasia, Immunohistochemistry, Ki-67 Antigen, Metaplasia, Middle Aged, Mitosis, Mutation, Precancerous Conditions, PTEN Phosphohydrolase, Receptors, Estrogen, Receptors, Progesterone, Time Factors
Abstract

Squamous morules are a common component of premalignant glandular lesions that are followed by glandular, rather than squamous, carcinomas. We tested the hypothesis that the appearance of glands associated with morules predicts cancer risk, and undertook molecular testing to determine the clonal and hormonal response properties of admixed squamous and glandular elements. A total of 66 patients with squamous morules in an index endometrial biopsy had follow-up clinical data (average follow-up: interval 31 months, 2.5 biopsies) showing development of carcinoma in 11% (7/66) of cases. The histological appearance of morule-associated glands in the index biopsy was significantly associated with this clinical outcome, with the majority (71%, 5/7) of cancer occurrences following an overtly premalignant lesion (endometrial intraepithelial neoplasia) with squamous morules. Eight endometrial intraepithelial neoplasias with squamous morules were examined by immunohistochemistry for estrogen and progesterone receptors and mitotic activity (Ki-67 antigen percent stained). Glandular components had abundant estrogen and progesterone receptors, and high levels of mitotic activity in all cases. In sharp contrast, all squamous morules were devoid of sex hormone receptors and had undetectable or extremely low-proliferation rates. When mutated, the same specific PTEN mutation was detected in squamous and glandular elements, indicating that both are of common lineage. The clinical and laboratory data are consistent with a model of morule biology in which squamous morules are a hormonally incompetent subpopulation of endometrial glandular lesions. Isolated morules might result from artifactual displacement from their native glandular context, or selective hormonally induced regression of the glandular but not squamous components over time. Subsequent cancer risk, as promoted by estrogens, is greatest when the glandular component has the appearance of endometrial intraepithelial neoplasia. Even isolated morules should be carefully followed, however, to exclude a coexisting undersampled, or occult, glandular lesion.

DOI10.1038/modpathol.2008.146
Alternate JournalMod Pathol
PubMed ID19180120
PubMed Central IDPMC2633489
Grant ListR01 CA092301 / CA / NCI NIH HHS / United States
R01 CA100833-05 / CA / NCI NIH HHS / United States
R01-CA92301 / CA / NCI NIH HHS / United States
R01 CA100833 / CA / NCI NIH HHS / United States
R01 CA100833-04 / CA / NCI NIH HHS / United States
R01 CA100833-01A1 / CA / NCI NIH HHS / United States
R01 CA092301-01A1 / CA / NCI NIH HHS / United States
R01 CA092301-04 / CA / NCI NIH HHS / United States
R01-CA100833 / CA / NCI NIH HHS / United States
R01 CA092301-03 / CA / NCI NIH HHS / United States
R01 CA100833-02 / CA / NCI NIH HHS / United States
R01 CA100833-03 / CA / NCI NIH HHS / United States
R01 CA092301-02 / CA / NCI NIH HHS / United States
R01 CA092301-05 / CA / NCI NIH HHS / United States

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