𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Simultaneous loss of E-cadherin and catenins in invasive lobular breast cancer and lobular carcinomain situ

✍ Scribed by de Leeuw, Wiljo J. F.; Berx, Geert; Vos, Carla B. J.; Peterse, Johannes L.; Van de Vijver, Marc J.; Litvinov, Sergey; Van Roy, Frans; Cornelisse, Cees J.; Cleton-Jansen, Anne-marie


Publisher
John Wiley and Sons
Year
1997
Tongue
English
Weight
461 KB
Volume
183
Category
Article
ISSN
0022-3417

No coin nor oath required. For personal study only.

✦ Synopsis


Loss of expression of the intercellular adhesion molecule E-cadherin frequently occurs in invasive lobular breast carcinomas as a result

of mutational inactivation. Expression patterns of E-cadherin and the molecules comprising the cytoplasmic complex of adherens junctions, -, -and -catenin, were studied in a series of 38 lobular breast carcinomas with known E-cadherin mutation status. The effect of loss of E-cadherin by mutational inactivation (or other mechanisms) on the expression of catenins was investigated. Complete loss of plasma membrane-associated E-cadherin expression was observed in 32 out of 38 invasive lobular carcinomas, for which in 21 cases a mutation was found in the extracellular domain of E-cadherin. In total, 15 frameshift mutations of small deletions or insertions, ranging from 1 to 41 bp, three non-sense mutations, and three splice mutations were identified. Mutations were scattered over the whole coding region and no hot spots could be detected. In all cases, simultaneous loss of E-cadherin and -and -catenin expression was found; in 50 per cent of these cases, additional loss of -catenin was observed. In six invasive lobular carcinomas, expression of both E-cadherin and catenins was retained. In none of these carcinomas was an E-cadherin mutation detected. Lobular carcinoma in situ adjacent to invasive lobular carcinoma showed simultaneous loss of E-cadherin and catenins in all the cases studied-remarkably, also, in four cases positive for E-cadherin and catenin expression in the invasive component. These results indicate that simultaneous loss of E-cadherin and -, -and -catenin may be an important step in the formation of lobular carcinoma in situ, as a precursor of invasive lobular breast cancer. Events additional to E-cadherin inactivation must be involved in the transition of lobular carcinoma in situ to invasive lobular carcinoma. 1997 John Wiley & Sons, Ltd.


πŸ“œ SIMILAR VOLUMES


An immunohistochemical examination of th
✍ Gonzalez, M. A.; Pinder, S. E.; Wencyk, P. M.; Bell, J. A.; Elston, C. W.; Nicho πŸ“‚ Article πŸ“… 1999 πŸ› John Wiley and Sons 🌐 English βš– 332 KB πŸ‘ 2 views

This study examines the expression of the cell-cell adhesion molecules E-cadherin and its associated proteins, the catenins and the matrix-cell adhesion molecules 1-and 2-integrins, in primary invasive breast carcinoma. Expression was assessed immunohistochemically on frozen sections by semi-quantit

Re-expression of E-cadherin, ?-catenin a
✍ Bukholm, I. K.; Nesland, J. M.; BοΏ½rresen-Dale, A.-L. πŸ“‚ Article πŸ“… 2000 πŸ› John Wiley and Sons 🌐 English βš– 249 KB πŸ‘ 1 views

Tumour cell invasion and metastasis are the processes which kill most cancer patients. Tumour cells with the greatest invasive and metastatic capacity may be those with the highest number of genetic aberrations. The present study has analysed the expression of several tumour-related proteins in both

Relation between aberrant Ξ±-catenin expr
✍ Rainy Umbas; William B. Isaacs; Pierre Paul Bringuier; Yong Xue; Frans M.J. Debr πŸ“‚ Article πŸ“… 1997 πŸ› John Wiley and Sons 🌐 French βš– 151 KB

It is now well documented that E-cadherin expression correlates inversely with tumor grade in various carcinomas including prostate cancer. We also demonstrated a statistically significant correlation between decreased E-cadherin expression and progression-free period in early stage patients treated

Cell cycle regulators in testicular canc
✍ Jirina Bartkova; Minna Thullberg; Ewa Rajpert-De Meyts; Niels E. Skakkebaek; Jir πŸ“‚ Article πŸ“… 2000 πŸ› John Wiley and Sons 🌐 French βš– 202 KB πŸ‘ 1 views

Cell cycle regulators govern cellular proliferation, modulate differentiation and, when defective, contribute to oncogenesis. Here, we examined expression of cyclins A, B1 and E, and cyclin-dependent kinase (CDK) inhibitors p18 INK4C (p18), p21 WAF1/Cip1 (p21) and p27 Kip1 (p27), in normal human adu