Role of Retinoblastoma Protein Family (Rb/p105 and Rb2/p130) Expression in the Histopathological Classification of Borderline Ovarian Tumors.

borderline ovarian tumors diagnosis pRb/p105 pRb2/p130 retinoblastoma protein family

Journal

Frontiers in medicine
ISSN: 2296-858X
Titre abrégé: Front Med (Lausanne)
Pays: Switzerland
ID NLM: 101648047

Informations de publication

Date de publication:
2020
Historique:
received: 18 08 2020
accepted: 15 10 2020
entrez: 2 12 2020
pubmed: 3 12 2020
medline: 3 12 2020
Statut: epublish

Résumé

Borderline ovarian tumors (BOT) are uncommon but not rare epithelial ovarian neoplasms, intermediate between benign and malignant categories. Emerging knowledge supports the notion that subtypes of borderline ovarian tumors comprise distinct biologic, pathogenetic, and molecular entities, precluding a single unifying concept for BOT. The identification of valuable markers for the diagnosis and classification of these tumors is in need. Among the molecular candidates, the Retinoblastoma (Rb) family members Rb/p105 and Rb2/p130 seem to play a pivotal role in ovarian cancer. In particular, Rb/p105, when in the unphosphorylated form, acts as a growth suppressor controlling cell cycle and tumor progression; whereas, the phosphorylated form activates gene transcription and cellular proliferation. While Rb/p105 is ubiquitously confined to the nuclei of cycling and quiescent cells, Rb2/p130 activity is also regulated by intracellular localization. According to this, Rb family members could represent a novel marker in diagnosis and classification risk for patients with BOT. In this study, we evaluated the expression and subcellular localization of proteins of the retinoblastoma (Rb) gene family in 65 ovarian borderline tumors. Statistically significant differences were found in nuclear and cytoplasmic expressions of Rb/p105 and Rb2/p130 according to different examined histotypes. In detail, the nuclear expression of Rb/p105 and Rb2/p130 was more frequently detected in serous (84.6%) than sero-mucinous (42.1%) and mucinous (50%) types. Conversely, the cytoplasmic expression of Rb2/p130 was not detected in serous tumors and frequently observed in mucinous subtypes (80%). Our findings suggest that Rb proteins do not play a key role in the tumor progression of serous borderline tumors since any cases showed cytoplasmic localization. By contrast, the observed higher cytoplasmic expression of Rb2/p130 in intestinal mucinous BOTs is indicative of Rb protein family involvement in the cancerogenesis pathway of mucinous ovarian tumors. Also, mucinous BOTs of intestinal-type, exhibiting low nuclear and high cytoplasmic levels of Rb2/p130 might potentially be considered a high-risk category of malignant evolution. Further studies on larger series are needed to clarify how BOTs could be stratified in different prognostic groups according to their Rb proteins immunohistochemical profile.

Identifiants

pubmed: 33262995
doi: 10.3389/fmed.2020.596226
pmc: PMC7686580
doi:

Types de publication

Journal Article

Langues

eng

Pagination

596226

Informations de copyright

Copyright © 2020 Masciullo, Valdivieso, Amadio, Santoro, Angelico, Sgambato, Boffo, Giordano, Scambia and Zannoni.

Références

Int J Gynecol Pathol. 1993 Apr;12(2):120-7
pubmed: 8463035
Cancer. 2004 Mar 1;100(5):1045-52
pubmed: 14983501
Hum Pathol. 2000 Jun;31(6):698-704
pubmed: 10872663
Gynecol Oncol. 2003 Mar;88(3):369-78
pubmed: 12648589
Am J Surg Pathol. 1999 Jun;23(6):617-35
pubmed: 10366144
J Biol Chem. 2003 May 23;278(21):19509-17
pubmed: 12621062
Am J Surg Pathol. 2000 Nov;24(11):1447-64
pubmed: 11075847
Hum Pathol. 2001 Apr;32(4):360-7
pubmed: 11331952
Cancer Res. 1994 Nov 1;54(21):5556-60
pubmed: 7923196
Int J Cancer. 1997 Aug 22;74(4):407-15
pubmed: 9291430
Oncol Rep. 2010 Dec;24(6):1411-8
pubmed: 21042734
Int J Gynecol Pathol. 2003 Apr;22(2):168-74
pubmed: 12649672
Clin Cancer Res. 2004 May 1;10(9):3098-103
pubmed: 15131049
Mol Cell Biol. 1997 Dec;17(12):7268-82
pubmed: 9372959
Cancer Genet Cytogenet. 1995 Nov;85(1):43-50
pubmed: 8536236
Best Pract Res Clin Obstet Gynaecol. 2017 May;41:15-30
pubmed: 28277307
Cancer Biol Ther. 2003 Nov-Dec;2(6):636-41
pubmed: 14688467
Mod Pathol. 2005 Feb;18 Suppl 2:S33-50
pubmed: 15761465
J Surg Oncol. 2005 Dec 15;92(4):337-43
pubmed: 16299808
Int J Gynecol Pathol. 1995 Jul;14(3):198-208
pubmed: 8600070
Appl Immunohistochem Mol Morphol. 2010 Dec;18(6):509-11
pubmed: 20661130
Virchows Arch. 2017 Feb;470(2):125-142
pubmed: 28025670
J Exp Clin Cancer Res. 2015 Nov 14;34:140
pubmed: 26576645
Hum Pathol. 2001 Jan;32(1):4-9
pubmed: 11172288
J Cell Biochem. 1996 Sep 1;62(3):418-30
pubmed: 8872613
Ann Oncol. 2016 Apr;27 Suppl 1:i20-i22
pubmed: 27141065
Hum Pathol. 2000 May;31(5):539-57
pubmed: 10836293
Cancer Res. 1996 May 1;56(9):2003-8
pubmed: 8616840

Auteurs

Valeria Masciullo (V)

Unità di Ginecologia Oncologica, Dipartimento Scienze della Salute della Donna, del Bambino e di Sanità Pubblica, Fondazione Policlinico Universitario A. Gemelli IRCCS, Roma, Italy.

Paola Valdivieso (P)

Unità di Ginecologia Oncologica, Dipartimento Scienze della Salute della Donna, del Bambino e di Sanità Pubblica, Fondazione Policlinico Universitario A. Gemelli IRCCS, Roma, Italy.

Giulia Amadio (G)

Unità di Ginecologia Oncologica, Dipartimento Scienze della Salute della Donna, del Bambino e di Sanità Pubblica, Fondazione Policlinico Universitario A. Gemelli IRCCS, Roma, Italy.

Angela Santoro (A)

Unità di Gineco-Patologia e Patologia Mammaria, Dipartimento Scienze della Salute della Donna, del Bambino e di Sanità Pubblica, Fondazione Policlinico Universitario A. Gemelli IRCCS, Roma, Italy.

Giuseppe Angelico (G)

Unità di Gineco-Patologia e Patologia Mammaria, Dipartimento Scienze della Salute della Donna, del Bambino e di Sanità Pubblica, Fondazione Policlinico Universitario A. Gemelli IRCCS, Roma, Italy.

Alessandro Sgambato (A)

Istituto di Patologia Generale, Università Cattolica del Sacro Cuore, Roma, Italy.

Silvia Boffo (S)

Department of Biology, College of Science and Technology, Sbarro Institute for Cancer Research and Molecular Medicine, Temple University, Philadelphia, PA, United States.

Antonio Giordano (A)

Department of Biology, College of Science and Technology, Sbarro Institute for Cancer Research and Molecular Medicine, Temple University, Philadelphia, PA, United States.

Giovanni Scambia (G)

Unità di Ginecologia Oncologica, Dipartimento Scienze della Salute della Donna, del Bambino e di Sanità Pubblica, Fondazione Policlinico Universitario A. Gemelli IRCCS, Roma, Italy.
Istituto di Clinica Ostetrica e Ginecologica, Università Cattolica del Sacro Cuore, Roma, Italy.

Gian Franco Zannoni (GF)

Unità di Gineco-Patologia e Patologia Mammaria, Dipartimento Scienze della Salute della Donna, del Bambino e di Sanità Pubblica, Fondazione Policlinico Universitario A. Gemelli IRCCS, Roma, Italy.
Istituto di Anatomia Patologica, Università Cattolica del Sacro Cuore, Roma, Italy.

Classifications MeSH