2018
DOI: 10.21873/anticanres.12627
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Stromal p16 Overexpression in Gastric-type Mucinous Carcinoma of the Uterine Cervix

Abstract: Stromal p16 expression of MC-G was significantly higher than that of normal cervix and other histological subtypes of adenocarcinoma and was associated with advanced stage, parametrial invasion, and lymphovascular invasion, reflecting the aggressive behavior of MC-G. Our observations suggest that stromal p16 expression is involved in the development and progression of MC-G.

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Cited by 17 publications
(21 citation statements)
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“…Sections (4-μm thick) cut from formalin-fixed, paraffin-embedded tissue blocks were placed onto Superfrost Plus glass slides (Thermo Fisher Scientific, Waltham, MA, USA). Thereafter, the sections were deparaffinized in xylene, rehydrated through a series of graded alcohols and immunohistochemically stained using an automated Ventana Benchmark XT (Ventana Medical Systems Inc.) as described by the manufacturer (7)(8)(9)(10)(11)(12)(13). Antigen was retrieved using CC1 Cell Conditioning Solution (Ventana Medical Systems Inc.).…”
Section: Methodsmentioning
confidence: 99%
See 1 more Smart Citation
“…Sections (4-μm thick) cut from formalin-fixed, paraffin-embedded tissue blocks were placed onto Superfrost Plus glass slides (Thermo Fisher Scientific, Waltham, MA, USA). Thereafter, the sections were deparaffinized in xylene, rehydrated through a series of graded alcohols and immunohistochemically stained using an automated Ventana Benchmark XT (Ventana Medical Systems Inc.) as described by the manufacturer (7)(8)(9)(10)(11)(12)(13). Antigen was retrieved using CC1 Cell Conditioning Solution (Ventana Medical Systems Inc.).…”
Section: Methodsmentioning
confidence: 99%
“…According to the recommendation of the LAST Standardization Project (6), the immunostaining profile of p16 was interpreted as block positive when p16 expression was horizontally continuous and strong, with nuclear or nuclear plus cytoplasmic staining. All other p16 immunostaining profiles, described as focal nuclear, wispy, bloblike, puddled, or scattered cytoplasmic staining were interpreted as patchy positive (9,(14)(15)(16)(17)(18)(19). in vivo 34: 2613-2621 (2020)…”
Section: Methodsmentioning
confidence: 99%
“…The slices were then deparaffinized and rehydrated with a xylene and alcohol solution. Immunostaining was performed using an automatic instrument [ 7 , 8 , 9 , 10 , 11 , 12 , 13 , 14 , 15 ]. After antigen retrieval, the slices were incubated with primary antibodies including p16 (prediluted, clone E6H4, Ventana Medical Systems, Oro Valley, AZ, USA) and Ki-67 (1:200, clone MIB-1, Dako, Glostrup, Denmark).…”
Section: Methodsmentioning
confidence: 99%
“…The 4 µm-thick, FFPE slices were de-paraffinized and rehydrated using a xylene and alcohol solution. Immunostaining was performed using automated instruments (Ventana Benchmark XT (Ventana Medical Systems) and or Dako Omnis (Dako, Carpinteria, CA, USA)) [1,[18][19][20][21][22][23][24][25][26]. After antigen retrieval, the slices were incubated with primary antibodies including pan-cytokeratin (pan-CK; 1:600, clone AE1/AE3, Dako), CK7 (Dako, 1:100, clone OV-TL 12/30, Dako), CK20 (1:100, clone Ks20.8, Dako), caudal type homeobox 2 (CDX2; 1:400, clone EPR2764Y, Cell Marque, Rocklin, CA, USA), paired box 8 (PAX8; 1:50, polyclonal, Cell Marque), estrogen receptor (ER; 1:150, clone 6F11, Novocastra, Leica Biosystems, Newcastle Upon Tyne, UK), progesterone receptor (PR; 1:100, clone 16, Novocastra), p53 (1:300, clone DO-7, Novocastra), p16 (prediluted, clone E6H4, Ventana Medical Systems), p63 (1:50, clone 4A4, Dako), and GATA-binding protein 3 (GATA3; 1:150, clone L50-823, Cell Marque).…”
Section: Immunohistochemistrymentioning
confidence: 99%