Antitumor effect of KT6124, a novel derivative of protein kinase inhibitor K-252a and its mechanism of action

Summary Novel derivatives of K-252a, (8R*,9S*,11S*)-(–)-9-hydroxy-9-methoxycarbonyl-8-methyl-2,3,9,10-tetrahydro-8, 11-epoxy-1H,8H,11H-2,7b,11a-triazadibenzo [a,g]-cycloocta[cde]trinden-1-one, an inhibitor of protein kinases and calmodulin-dependent phosphodiesterase, were synthesized and evaluated for their antitumor activity in vitro and in vivo. Of ten derivatives tested, four were active against the P388 murine leukemia i. p.-i. p. system, although K-252a was inactive. Among these derivatives, KT6124 was selected for further biological evaluation studies because its efficacy was the highest. KT6124 was also active against sarcoma 180 and B16 melanoma. It exerted a relatively broad spectrum of antiproliferative activity against 20 human tumor cell lines in vitro. To determine the mechanism(s) of action underlying the antitumor activity of KT6124, we tested the drug for inhibition of protein kinases, including Ca²⁺-and phospholipid-dependent protein kinase (PKC), in intact A431 human epidermoid carcinoma cells in comparison with the PKC-inhibitory activity of K-252a. KT6124 did not antagonize the action of phorbol 12-myristate 13-acetate (PMA) in A431 cells, whereas K-252a did, suggesting that KT6124 may not act on protein kinases in the cells. The interaction of KT6124 with DNA in living cells was examined by the alkaline elution method. KT6124 apparantly exhibited DNA scission both dose-and time-dependently in the target cells. The DNA breakage was dependent on proteinase K treatment, suggesting its possible interaction with DNA-related enzyme(s). These results indicate that KT6124 exerts antitumor activity by acting on DNA or on DNA-related enzyme(s) in tumor cells rather than via the inhibition of protein kinases.     

Classification of Diabetes Mellitus by Studies of C-Peptide Secretory Capacity

Residual pancreatic B-cell function was investigated in children with diabetes mellitus in whom classification of the type of disease was difficult at the first visit. Intravenous glucagon tests were performed at the first visit and subsequently, the C-peptide responses compared. Based on our data on a limited number of patients, we propose C-peptide concentrations of 3.0 to 3.5 ng/ml at the peak or at 6 min after injection of glucagon, as the critical level which distinguishes non-insulin dependent from insulin-dependent diabetes mellitus. However, the degree of obesity, clinical stage and other factors also need to be considered in the classification of diabetes mellitus.     

THE COMPARATIVE MERITS OF VARIOUS COMPLEMENTS AND AMBOCEPTORS IN THE SERUM DIAGNOSIS OF SYPHILIS

1. The maximum activity of an antihuman hemolytic amboceptor may be obtained by employing the homologous or heterologous complement, according to the variable relations existing between the species furnishing the amboceptor and the one supplying the complement. Thus, some amboceptors are best reactivated by the complement of the same species, while others may act most strongly when reactivated with the complements of certain suitable heterologous species. 2. From the above it is clear that the complementary activity of a given serum may be very variable according to the varieties of amboceptors employed. In expressing the complementary activity of a serum, the species of the host of the amboceptor must always be stated. Thus, one serum may have many different complementary titers according to the amboceptors used. A similar variation in the titers of the amboceptors occurs when a variety of complements are employed. 3. Certain species of animals (pig and sheep) yield sera which are comparatively poor in reactivating most varieties of antihuman amboceptors. The complements of these species deteriorate rapidly. 4. The serum of chicken contained but little complement for the amboceptors derived from the mammalia, while the amboceptor from the chicken was only poorly, or not at all, reactivable by the complements contained in the mammalian sera. The serum of pig was the only variety which reactivated this amboceptor in a fair degree. 5. For the fixation tests guinea pig complement is the most favorable. This complement is also the most active and durable of those which have been studied. The complements of pig and sheep are quite fixable, but their weakness and rapid deterioration render them unsuitable for fixation purposes. Rabbit complement is quite active but is not easily fixable. Goat complement is, as already stated, difficult to fix, in spite of its strong complementary activity. The other complements are unsuitable because of their feeble complementary activity. 6. For fixation tests the antihuman amboceptors produced in the rabbit and guinea pig are suitable. They are, moreover, very active and do not cause the phenomenon of non-fixation. The amboceptors from other animals are unsuitable, as we cannot find a complement which strongly reactivates them. The amboceptor from the goat is unsuitable because of the danger of masking the fixation phenomenon by subsequent hemolysis. 7. In summing up, we arrive at the conclusion that the rabbit is the best animal for producing antihuman amboceptor, and the guinea pig for supplying complement. The guinea pig produces a good amboceptor, but its small size renders it second in choice. So far, no other animals have been found useful for the fixation experiments.     

Ascending contraction and descending relaxation in the distal colon of mice lacking interstitial cells of Cajal.

Recently an essential role of interstitial cells of Cajal (ICC) within myenteric plexus (ICC-MY) was suggested in ascending contraction and descending relaxation in the mouse ileum. The role of ICC in these neural reflexes was examined in the distal colonic segments prepared from the wild type and c-kit mutant, W/W(V) mice, in the present study. Localized distension of the segments from the wild type mice by using a small balloon resulted in ascending contraction and descending relaxation. In the segments from the mutant mice, localized distension also induced these neural reflexes similar to those observed in the wild type mice. Immunohistochemical examination demonstrated that ICC-MY and ICC present in muscle layers (ICC-IM) were severely disrupted in the mutant mouse, but only ICC, present within submucosal plexus (ICC-SMP), remained unchanged. In the small strips with ICC-SMP absent prepared from the mutant mouse, electrical field stimulation induced contraction or relaxation in the absence or presence of atropine, respectively. It was suggested that ICC have no important role in the ascending and descending neural reflexes in the mouse distal colon, this is in direct contrast to the role of ICC-MY in the ileum.     

Double congenital bronchoesophageal fistulae in an adult

We report adult congenital bronchoesophageal fistula with both symptomatic fistula and asymptomatic one. A 56-year-old woman with a history of cough after drinking fluids was diagnosed as bronchoesophageal fistula by upper gastrointestinal series that showed a diverticulum in the middle portion of the esophagus with a fistula between the esophagus and right lower lung. Esophagoscopy revealed an orifice of the fistula located 27 cm from the incisors. Computed tomography showed chronic inflammatory change with bronchiectasis in the S6 segment of the right lung. The patient underwent video assisted thoracic surgery that identified two fistulae without missing a symptomatic one, and both were successfully resected. The fistulae were lined by squamous epithelium and smooth muscle without evidence of malignancy, infection or chronic inflammation that were histologically compatible with congenital fistulae.