When incubated in preconditioned medium, i.e. spent media from the hepatocellular carcinoma (PLC/PRF/5) cell cultures, human embryonic liver (HEL) cells differentiate and acquire oncologic phenotypes. This is caused by transcriptional alterations in fetal gene expression. This occurs when hepatocytes are proliferating rapidly and secreting alpha fetoprotein (AFP), and later when the quiescent state is reached with secretion of albumin (ALB). The present studies examined the parameters signaling oncologic transformation during liver cell differentiation in the conditioned medium. mRNAs coding for AFP, ALB and HBsAg were isolated from HEL, adult liver cells (ADLC) and from PLC/PRF/5 cells, respectively. cDNA molecules complementary to these polysomal mRNA molecules were constructed and labeled with 32P. These tracers were used to quantitate changes in cellular mRNA • AFP, mRNA • ALB and mRNA·HBsAg directly by DNA molecular hybridization during HEL cells cultivation in the preconditioned medium. Under these conditions, the changes in cellular mRNA·HBsAg and mRNA • AFP correlated with an increased tumorigenicity in athymic Nu/Nu mice, membrane galactosyltransferase and phospho-tyrosine kinase activities.
L o t h a r H. Hussman, M.D., Charles S i r a k i , M.D.; and B e r t h o l d O s t e r t a g , M.D. ABSTRACT. S p e c i f i c p i c t u r e s i n A-scope u l t r a s o n o g r a m s a r e r e l a t e d d i r e c t l y t o b i o l o g i c a l changes i n t h e b r a i n , by o u r f i n d i n g s . T h i s r e l a t i o n s h i p a p p e a r s i n edema, c i r c u l a t o r y d i s t u r ba n c e s , a n a t o m i c a l a b n o r m a l i t i e s , d e g e n e r a t i v e c e r e b r a l d i s e a s e , normal p r e s s u r e h y d r o c e p h a l u s , space-occupying l e s i o n s , b r a i n damage i n s e v e r e l y burned p a t i e n t s , c o n v u l s i v e d i s o r d e r s , and even i n b r a i n d e a t h . Experiments done w i t h M e t r a z o l and e l e c t r o s h o c k have e l u c i d a t e d t h e s e rel a t i o n s h i p s as t o c o n v u l s i v e d i s o r d e r s and b r a i n death; U l t r a s o n i c d i a g n o s i s t h e r e f o r e e x t e n d s beyond t h e s o -c a l l e d s h i f t of t h e m i d l i n e s t r u c t u r e s . Changes i n e l a s t i c p a r a m e t e r s ( r i g i d i t y and f l a c c i d i t y ) and dynamics of c i r c u l a t i o n and v e n t r i c l e p u l s a t i o n s are r e l e v a n t f a c t o r s modif i e d by t i s s u e p o l a r i z a t i o n . W e b e l i e v e o u r f i n d i n g s open new avenues f o r c l i n i c a l u s e of echoencephalography, which some have t h o u g h t had r e a c h e d i t s l i m i t s i n merely d e t e r m i n i n g s h i f t s i n t h e m i d l i n e complex. White i n 1973 w r o t e t h a t i t i s d i f f i c u l t t o p r ed i c t what e f f e c t a x i a l tomography w i l l have upon t h e f u t u r e development of u l t r a s o n i c encephalography, b u t w e today have no doubt t h a t t h e f u t u r e i s i n e e d v e r y b r i g h t and t h a t t h e EM1 s c a n n e r need n o t f r i g h t e n us i n t h e l e a s t . On t h e c o n t r a r y , we a r e v e r y much encouraged and q u i t e i n agreement w i t h White, who a l s o c l a i m s i n t h e same p a p e r t h a t "range v a r i a t i o n s from s i n g l e i n t r a c r a n i a l i n t e r f a c e s s h o u l d c o n t i n u e t o b e i n v e s t i g a t e d " and t h a t i n a d d i t i o n t o t h e r e g i s t r at i o n of slow p r e s s u r e changes, more i n f o r m a t i o n of c l i n i c a l v a l u e can b e a c q u i r e d by t h i s s i m p l e noni n t r u s i v e t e c h n i q u e . " T h e r e f o r e w e can b e much more a f f i r m a t i v e and p o s i t i v e i n o u r c o n v i c t i o n t h a t , a l l i n a l l , " l a r g e and rewarding f i e l d s " i n t h e u s e of d i a g n o s t i c u l t r asonography s t i l l a w a i t c u l t i v a t i o n . I t i s h e l p f u l t o compare u l t r a s o n i c t r a n s -s k u l l v i s u a l i z a t i o n w i t h t h e t e c h n i q u e of computerized a x i a l tomography. During a r e c e n t Chicago symposium on t h i s new s c a n n i n g d e v i c e , i t becam...
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
customersupport@researchsolutions.com
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.
Copyright © 2025 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.