Sabato 27 ottobre 2012 - Pacini Editore
Sabato 27 ottobre 2012 - Pacini Editore
Sabato 27 ottobre 2012 - Pacini Editore
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COmuNiCaziONi ORali<br />
patients who had undergone cystoprostatectomy for bladder cancer<br />
(controls). Immunostainings and confocal microscopy were<br />
used to visualize SLUG expression at the protein level.<br />
Results. SLUG gene expression levels were significantly<br />
(P < 0.05) lower in the neoplastic (with no appreciable difference<br />
between low and high-grade PCa) versus normal prostatic<br />
epithelia (~12 times in low grade, ~16 times in high grade) and in<br />
neoplastic versus normal stroma (~4 times in both grades).<br />
SLUG was predominantly expressed in the stromal rather than<br />
the epithelial compartment, with higher levels in the neoplastic<br />
stroma. The mean expression level of SLUG in normal samples<br />
from the untreated patients was not significantly different to that<br />
obtained in normal samples from controls.<br />
Immunostainings showed that, in the normal prostate glands,<br />
both basal and luminal secretory cells strongly expressed SLUG<br />
in their nuclei, whereas SLUG staining ranged from very weak<br />
to moderate in the neoplastic glands. SLUG expression was inversely<br />
related to that of the cell cycle regulator cyclin D1, and<br />
the proliferation marker Ki-67.<br />
Lastly, ADT generally enhanced SLUG expression in the stroma,<br />
particularly in that of low-grade PCa.<br />
Conclusions. These preliminary findings suggest that, as observed<br />
in PCa cell lines (3), in the human prostate tissues, SLUG<br />
may inhibit neoplastic epithelial cell proliferation rather than act<br />
as an EMT promoter. It may also have a different role in the PCaassociated<br />
stroma, whose response to ADT may have important<br />
clinical and pathological implications. All these issues are the<br />
subject of ongoing investigation in our laboratories.<br />
references<br />
1 Nieto MA, Sargent MG, Wilkinson DG, et al. Control of cell behavior<br />
during vertebrate development by Slug, a zinc finger gene. Science<br />
1994;264:835-9.<br />
2 Barrallo-Gimeno A, Nieto MA. The Snail genes as inducers of cell<br />
movement and survival: implications in development and cancer.<br />
Development 2005;132:3151-61.<br />
3 Liu J, Uygur B, Zhang Z, et al. Slug inhibits proliferation of human<br />
prostate cancer cells via downregulation of cyclin D1 expression.<br />
Prostate 2010;70:1768-77.<br />
Pathological staging of uterine cervical carcinoma<br />
after neoadjuvant chemotherapy: a predictor<br />
of survival<br />
V.G. Vellone1 , D. Lorusso2 , V. Masciullo2 , G. Amodio2 , G. Chiarello1<br />
, E.D. Rossi1 , G. Fadda1 , G. Scambia1 , G.F. Zannoni2 1 Istituto di Anatomia ed Istologia Patologica, Policlinico A. Gemelli, Università<br />
Cattolica S.Cuore, Roma; 2 Istituto di Ostetricia e Ginecologia,<br />
Policlinico A. Gemelli, Università Cattolica S.Cuore, Roma<br />
Background. Radio-chemotherapy represents a relevant therapeutic<br />
option for cervical carcinoma. Surgical removal of uterus,<br />
ovaries, lymph nodes and peritoneal sampling after the neoadjuavant<br />
treatment give us the unique opportunity to evaluate the real<br />
ammount of the residual, its anatomic location and its impact on<br />
overall survival. A staging method is proposed and its implication<br />
in prognosis is investigated.<br />
Materials and methods. Study population: 114 cervical cancer<br />
patients (stage IB-IV FIGO)<br />
Treatment: platinum based chemotherapy with concomitant<br />
external beam radioterapy and then radical hysterectomy, lyphadenectomy<br />
and peritoneal sampling<br />
Local response classificated as follow 1 2 :<br />
pR0: Pathological Complete Response<br />
pR1: Pathological Partial Response<br />
pR2: Pathological No Response.<br />
325<br />
All patients were re-staged according to ypTNM and FIGO staging<br />
and then combined with pR as follow:<br />
No Residual Disease (NRD): pR0 Stage 0<br />
Minimal Residual Disease (MRD): pR1 Stage IA and IB; pR2<br />
Stage IA<br />
Local Residual Disease (LRD): pR1 Stage IIA and IIB; pR2<br />
Stage IB, IIA, IIB<br />
Metastatic Disease (MD): any pR Stage III and IV<br />
Mean follow-up: 39 months<br />
Results. 46 patients resulted NRD; 25 MRD; 23 LRD; 20 MD.<br />
NRD patients showed a significant advantage in suvival if compared<br />
to LRD (p < 0,001) and MD (p < 0,001). No significant<br />
difference were observed with MRD<br />
LRD showed a slight better survival if compared to MD (p = 0,1).<br />
Conclusions. A complete pathological staging confirmed its crucial<br />
role in risk stratification. Furthermore it could be useful for planning<br />
a second line treatment after surgery in patient with residual.<br />
referencies<br />
1 Zannoni GF, Vellone VG, Carbone A. Morphological effects of radiochemotherapy<br />
on cervical carcinoma: a morphological study of<br />
50 cases of hysterectomy specimens after neoadjuvant treatment. Int J<br />
Gynecol Pathol 2008;<strong>27</strong>:<strong>27</strong>4-81.<br />
2 Zannoni GF, Vellone VG. Accuracy of Papanicolaou smears in cervical<br />
cancer patients treated with radiochemotherapy followed by radical<br />
surgery. Am J Clin Pathol 2008;130:787-94.<br />
Clinical, pathological and molecular prognostic<br />
factors for non-endometrioid (type II) endometrial<br />
carcinoma<br />
V.G. Vellone1 , A. Fagotti2 , D. Gallo2 , C. Bottoni2 , L. Santoro1 ,<br />
E.D. Rossi1 , G. Fadda1 , G. Scambia1 , G.F. Zannoni2 1 Istituto di Anatomia ed Istologia Patologica, Policlinico A.Gemelli, Università<br />
Cattolica S.Cuore, Roma; 2 Istituto di Ostetricia e Ginecologia,<br />
Policlinico A.Gemelli, Università Cattolica S.Cuore, Roma<br />
Background. Non Endometrioid Endometrial Carcinoma (NEC)<br />
are an heterogeneus group of neoplasms with a notorius highly<br />
malignant behaviour, with different features and a worse prognosis<br />
if compared to conventional endometrioid carcinomas 1 .<br />
The impact in prognosis of a series of clinical, pathological and<br />
molecular markers is investigated.<br />
Materials and methods. Study population: 28 non endometrioid<br />
endometrial carcinoma patients treated withradical hysterectomy,<br />
lymph adenectomy and peritoneal sampling.<br />
Mean Follow up duration: 32 months<br />
Impact in overall survivall of Patients age, Tumor size, % of<br />
Myometrial Invasion, Lymph nodes metastases, extralimphonodal<br />
metastases, Stage, ER, PR, Her2/neu, Ki67, p53, bcl-2 is<br />
investigated<br />
Results. NEC confirmed its fame of deadly disease: half of the<br />
patients died of the disease. We found no prognostic significance<br />
for Age, Tumor size, % of Myometrial Invasion, Lymph nodes<br />
metastases, extralimphonodal metastases, Stage, ER, PR, Ki67,<br />
p53, bcl-2 (p > 0,05).<br />
Only positivity for Her2/neu (2+ FISH+ or 3+) identified a sub<br />
population of cases with a worse prognosis (p = 0,03).<br />
Conclusions. This finding confirm the aggressiveness of these<br />
neoplasms but rise new opportunities in target terapies for these<br />
unlucky patients.<br />
references<br />
1 Zannoni GF, Vellone VG, Arena V, et al. Does high-grade endometrioid<br />
carcinoma (grade 3 FIGO) belong to type I or type II endometrial<br />
cancer? A clinical-pathological and immunohistochemical study. Virchows<br />
Arch 2010;457:<strong>27</strong>-34.