SVIBOR - Papers - project code: 1-08-303

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SVIBOR

SVIBOR - Collecting Data on Projects in Croatia


Published papers on project 1-08-303


Quoted papers: 3
Other papers: 19
Total: 22


  1. Type of paper: Paper in book

    Title:

    Authors:
    Bašić, Ivan (2406)
    Grdina, D.J.
    Lyons, T.
    Editors
    Nygaard, Oddvar
    Upton, Arthur
    Publisher: Plenum Press
    ISBN: 0-306-44056-3
    Year: 1991
    Pages: from 297 to 301
    Number of references: 7
    Language: engleski

  2. Type of paper: Paper in book

    Title: Antimetastatic activity of bee venom and water - soluble derivative of propolis in mice

    Authors:
    Bašić, Ivan (2406)
    Ćurić, Stipica (108013)
    Tadić, Zoran (143012)
    Oršolić, Nada
    Sulimanović, Đuro (45465)
    Editors
    Cochard, Jean - Paul
    Publisher: International Apicultiral Organization
    Year: 1996
    Number of references: 11
    Language: engleski

  3. Type of paper: Paper in journal

    Title:

    Authors:
    Kataoka, Y.
    Bašić, Ivan (2406)
    Perrin, J.
    Grdina, D.J.
    Journal: International Journal of Radiation Biology
    Number: 3
    ISSN: 0020-7616
    Volume: 61
    Year: 1992
    Pages: from 387 to 392
    Number of references: 27
    Language: engleski
    Summary: The antimutagenic effects of the radiation protective agent S - 2- (3 - aminopropylamino)ethylphosphorothionic acid (WR - 2721)were studied against fission - spectrum - netron and 60 Co gammaray - induced mutagenesis in mice. Mutagenesis at the hypoxantine- guanine phosphoribosyl transferase (HPRT) locus was measured 56days following whole - body irradiation with JANUS neutrons(single doses, 50 - 150 cGy) or 60 Co photons (single doses, 250- 750 cGy). Splenic T lymphocytes from B6CF1 mice were grown inround - bottomed 96 - microwell culture plates with or withoutthe selective agent 6 - thioguanine (6 - TG). Mutant frequency,as a result of exposure to neutrons or 60 Co photons, increased100-fold with dose. Doses of 150 cGy neutrons and 750 cGy 60 Cophotons were equally mutagenic. When animals were injected withWR - 2721 at a dose of 400 mg/kg body weight, i.p., 30 min beforewhole-body irradiation with JANUS neutrons or 60 Co photons,mutant frequencies were significantly reduced at all radiationdoses (i.e. protection factors of 1.4 and 2.4, respectively.Thus, the aminothiols are effective antimutagens. a novelclinical application of these compounds could be in their use toprotect against radiation - and/or chemotherapy induced genotoxicdamage to normal cells.

  4. Type of paper: Paper in journal

    Title:

    Authors:
    Ćurić, Stipica (108013)
    Oršolić, Nada
    Krsnik, Boris (23981)
    Balenović, Tomislav (1771)
    Valpotić, Ivica (66266)
    Sulimanović, Đuro (45465)
    Bašić, Ivan (2406)
    Journal: Stočarstvo
    Number: 3
    ISSN: 638 -1394
    Volume: 47
    Year: 1993
    Pages: from 131 to 136
    Number of references: 11
    Language: engleski
    Summary: The effect of honeybee venom on humoral (gamma globulin and totalprotein levels) and cellular immune responses (weight andcellularity of spleen and lymph nodes) was tested in CBA mice.Bee venom was injected subcutaneously into the left footpad at adose of 0.15, 0.30 or 0.60 mg per mouse, respectively. Mean gammaglobulins and total protein values were significantly elevated (P< 0.05) in mice treated with 0.15 mg or 0.30 mg of bee venom,respectively, compared to those recorded in nontreated controls.Weight of the left popliteal lymph node (LPLN) was significantlyhigher (P < 0.01) in mice given 0.30 mg or 0.60 mg of bee venomthan that of the controls. the cellularity of LPLN in bee venom -treated mice was much greater (P < 0.05; < 0.01) when compared tothe control values. However, no differences in weight andcellularity of the popliteal lymph node were noticed in micetreated with identically with propolis, used as an antigen. Therewere no differences in weight or cellularity of spleen betweentreated and control mice.

  5. Type of paper: Paper in journal

    Title:

    Authors:
    Šamija, Mirko (66200)
    Eljuga, Damir (87925)
    Košuta-Špoljar, Dunja (81851)
    Gerenčer, Marijan
    Bašić, Ivan (2406)
    Journal: Libri Oncologici
    Number: 3
    ISSN: 0300-8142
    Volume: 20
    Year: 1991
    Pages: from 131 to 133
    Number of references: 13
    Language: engleski
    Summary: The effect of primary local irradiation and IL - 2 preparationadministration on the number of spontaneous metastases to thelungs of Y-59 rats was studied. Spontaneously formedtransplantable anaplastic carcinoma (ACA) in Y-59 rats was usedin the experiment. On the 6th day following inoculation of 5 x 105 ACA cells into the foot of a posterior leg, the entire footpadwith developing tumor was irradiated a single dose of 20 Gy quickelectrons. Then, a group of animals was intraperitoneallyinjected 500 IU IL - 2 preparation each 12 hours through 3 days.The animals were sacrificed on the 22nd day when the number ofmetastases to the lungs was determined. Observed was that thenumber of spontaneous metastases was considerably smaller inlocally irradiated and intraperitoneally IL - 2 preparationinjected animals.
    Keywords: primary tumor, interleukin 2, antimetastatic effect

  6. Type of paper: Paper in journal

    Title:

    Authors:
    Grdina, D.J.
    Kataoka, Y.
    Bašić, Ivan (2406)
    Perrin, J.
    Journal: Carcinogenesis
    Number: 5
    ISSN: 0143-3334
    Volume: 13
    Year: 1992
    Pages: from 811 to 814
    Number of references: 32
    Language: engleski
    Summary: An "in vitro" T lymphocyte cloning technique has been applied tostudy the effects of JANUS fission - spectrum neutron irradiationand radioprotector S - 2 - (3 -aminopropylamino)ethylphosphorothioic acid (WR - 2721) on thesubsequent development of somatic mutations at the hypoxantine -guanine phopshoribosyl transferase (hprt) locus in hybrid B6CF1male mice. In control studies performed to establish an "invitro" cloning technique, the mutant frequencies of splenic Tlymphocytes, as result of exposure to a 100 cGy dose of neutrons,increased with time from a control level of 9 X 10 -7 to maximumvalue of 1.7 X 10 -5 at 56 days following irradiation between 56and 150 days after irradiation mutant frequencies were observedto plateau and remain stable. all suqsequent determinations wereperformed at 56 days following the experimental treatment ofanimals. WR - 2721 at a dose of 400 mg/kg was effective inprotecting against the induction of HPRT mutants (i.e. mutantfrequency reduction factor, MFRF)following the largest dose ofneutrons used (i.e. 150 cGy), whether it was administered i.p. 30before, 5 minutes after, 3 hours after or 3 times at 3, 24 and 48hours after, as evidenced by MFRFs of 6.0, 6.6, 4.8 and 5.8respectively. Antimutagenic effectiveness of WR - 2721administered 30 minutes prior to irradiation was unaffected, evenwhen the dose was reduced to 200 mg/kg, MFRF = 7.0; 100 mg/kg,MFRF = 3.8; and 50 mg/kg, MFRF = 8.9. These findings confirm ourearlier report using the radioprotector N - (2 - mercaptoethyl) -1,3 - diaminopropane (WR - 1065) under "in vitro" conditions, anddemnonstrate that these agents can be used as effectiveantimutagens even when they are administered up to 3 hoursfollowing radiation exposure.

  7. Type of paper: Paper in journal

    Title:

    Authors:
    Tadić, Zoran (143012)
    Journal: Libri Oncologici
    Number: 3
    ISSN: 0300-8142
    Volume: 21
    Year: 1992
    Pages: from 153 to 159
    Number of references: 13
    Language: engleski
    Summary: Hepatitis B virus is etiologic agent of acute hepatitis and isconsidered to be a major factor in hepatocellular carcinomainitiation. Here, the tranforming capability of normal andmutated HBV X gene was investigated. NIH 3T3 cells weretransfected with plasmids carrying normal X gene and frameshiftmutant in which only small part is translated correctly. Bothconstructs were driven by Rous sarcoma virus LTR promoter. Thetransformed phenotype was tested in focus - forming assay andability to grow in semisolid medium (soft agar). In both testmutated HBV X gene showed significantly greater transformingcapability than its normal counterpart. The possible mechanismsof these observation are discussed with the special emphasis onadditional open reading frames within the X ORF.
    Keywords: hepatitis B virus, gene X, transformation

  8. Type of paper: Paper in journal

    Title:

    Authors:
    Ćurić, Stipica (108013)
    Tadić, Zoran (143012)
    Valpotić, Ivica (66266)
    Sulimanović, Đuro (45465)
    Bašić, Ivan (2406)
    Journal: Veterinarski Arhiv
    ISSN: 618 -006
    Volume: 62
    Year: 1992
    Pages: from 31 to 35
    Number of references: 10
    Language: engleski
    Summary: The effect of honeybee venom on the tumor growth and metastasisformation in mice was studied. Bee venom was injected into miceeither subcutaneously (s.c.) or intravenously (i.v.) at differentdoses. The tumor was transplantable mammary carcinoma (MCA)weakly immunogenic to the syngeneic CBA mouse. The tumor wasgenerated by injecting 10 5 MCA cells i.v.. When the tumor cellswere injected s.c. into the footpad immediately after bee venom,the growth of the tumor was supressed regardless of dose of thevenom. Survival of the mice treated with 0.30 mg of bee venom wasprolonged as compared to the controls. the number of lungmetastases in the mice treated i.v. with 0.15 or 0.075 mg of beevenom was significantly lower (P < 0.001) than that in nontreated mice. However, both doses of bee venom given s.c. did notreduce the number of lung metastases indicating that theantitumor effect of the venom could be highly dependent on theroute of injection.
    Keywords: murine mammary carcinoma, antitumor and antimetastatic activity, honeybee venom

  9. Type of paper: Paper in journal

    Title:

    Authors:
    Ćurić, Stipica (108013)
    Valpotić, Ivica (66266)
    Sulimanović, Đuro (45465)
    Bašić, Ivan (2406)
    Journal: Veterinarski Arhiv
    ISSN: 618 -006
    Volume: 62
    Year: 1992
    Pages: from 43 to 47
    Number of references: 7
    Language: engleski
    Summary: The effect of honeybee venom on humoral (gamma globulin and totalprotein levels) and cellular immune responses (weight andcellularity of spleen and lymph nodes) was tested in CBA mice.Bee venom was injected subcutaneously into the left footpad at adose of 0.15, 0.30 or 0.60 mg per mouse, respectively. Mean gammaglobulins and total protein values were significantly elevated (P< 0.05) in mice treated with 0.15 mg or 0.30 mg of bee venom,respectively, compared to those recorded in nontreated controls.Weight of the left popliteal lymph node (LPLN) was significantlyhigher (P < 0.01) in mice given 0.30 mg or 0.60 mg of bee venomthan that of the controls. the cellularity of LPLN in bee venom -treated mice was much greater (P < 0.05; < 0.01) when compared tothe control values. However, no differences in weight andcellularity of the popliteal lymph node were noticed in micetreated with identically with propolis, used as an antigen. Therewere no differences in weight or cellularity of spleen betweentreated and control mice.
    Keywords: honeybee venom, immune response, CBA mice

  10. Type of paper: Paper in journal

    Title:

    Authors:
    Tadić, Zoran (143012)
    Bašić, Ivan (2406)
    Journal: Croatian Journal of Gastroenterology and Hepatology
    Number: 4
    ISSN: 0353-9296
    Volume: 1
    Year: 1992
    Pages: from 175 to 178
    Number of references: 10
    Language: engleski
    Summary: Using retroviral vector, an efficient expression of the HBV Xgene was achieved. Molecular analysis of isolated cellular DNAshowed integrity of the provirus and Northern hybridizationconfirmed functionality of the integrated provirus. The tests oftransformed phenotype revealed the mutated HBV X gene totransform NIH 3T3 cells more efficiently that the wild type gene.
    Keywords: hepatitis B virus, DNA viral, genetic vectors, retroviridae

  11. Type of paper: Paper in journal

    Title:

    Authors:
    Eljuga, Ljerka
    Šamija, Mirko (66200)
    Eljuga, Damir (87925)
    Košuta-Špoljar, Dunja (81851)
    Bašić, Ivan (2406)
    Journal: Libri Oncologici
    Number: 3
    ISSN: 0300-8142
    Volume: 22
    Year: 1993
    Pages: from 177 to 181
    Number of references: 15
    Language: engleski
    Summary: The effect of lymphokine - activated killer (LAK) cells andrecombinant interleukin - 2 (rIL - 2) on the development ofpulmonary metastases of anaplastic cxarcinoma (ACA) in Y59 ratand on the survival of animals was studied. LAK cells (10 7) weregiven intravenously (i.v.) 4 days after i.v. injction of 3 X 10 3tumor cells.Immediately after the administration of LAK cellsanimals received i.p. an injection containing 100 IU of rIL - 2.Injections of rIL - 2 were done given for 3 consecutive days in 8hour intervals. The combined use of LAK cells and rIL - 2produced a pronounced antimetastatic activity and significantlyextended the survival of animals.
    Keywords: metastasis, rIL - 2, LAK cells

  12. Type of paper: Paper in journal

    Title: Developing concept of macrophage activation

    Authors:
    Verstovšek, Srđan
    Bašić, Ivan (2406)
    Journal: Libri Oncologici
    Number: 1
    ISSN: 0300-8142
    Volume: 24
    Year: 1995
    Pages: from 9 to 17
    Number of references: 54
    Language: engleski
    Summary: The functional potential of macrophages is one of the major criteria used to differentiate morphologically mature tissue macrophages. However, the spectrum of macrophage functional potential is broad and it can be expressed in a number of different ways upon exposure to one or more different stimuli in the tissue environmrent. It is discussed that the concept of activation in reality encompasses multiple states of macrophage functional potential, multiple activation pathways and multiple stages of activation. Thus despite the fact that mononuclear phagocytes belong to a single system, it is suggested that they display varied functional properties based on the local environmental pressures under which they develop, including regulation by cells of other systems, and, further that their responsiveness to extracellular signals is dependent upon their developmental stage in the activation process at the time the signal is applied.
    Keywords: macrophages, heterogeneity, activation

  13. Type of paper: Summary in proceedings

    Title: Effect of local administration of cytostatic and biological response modifiers (BRM) on liver metastasis of a colon tumor in the rat

    Authors:
    Oršolić, Nada
    Kujundžić, Milan (168490)
    Kaštelan, Maja
    Tadić, Zoran (143012)
    Ćurić, Stipica (108013)
    Bašić, Ivan (2406)
    Editors
    Gomerčić, Hrvoje
    Proceedings title: Zbornik sažetaka priopćenja petog kongresa biologa Hrvatske s međunarodnim sudje
    Language: hrvatski
    Place: Zagreb
    Year: 1994
    ISBN/ISSN: 953-6241-01-3
    Pages: from 162 to 163
    Meeting: Peti kongres biologa Hrvatske s međunarodnim sudjelovanjem
    Held: from 10/03/94 to 10/07/94
    Summary: Using a model of artificial liver metastasis of a weakly immunogeneic colon adenocarcinoma of the rat, the antitumor effect of intrahepatally administered high doses of doxorubicin or 5-FU combined with intrasplenic ( IS ) administration of biological rensponse modifiers ( levamisole, IL-2, or a lyophilysed extract of the plant Caucalis platicarpos L.) was studied.Animal that received cytostatics aaalone survived significantly longer than untreated control; the increase of the dose resulted in better survival and the lesions to bone marrow in these animals were not augmented.Complete disappearance of liver metastasis was frequently observed when administration of cytostatics combined with either of BRM.In addition, BRM combined with cytostatics prevented the dissemination of tumor cells to other organs.Immunological parameters such as NK activity and response to mitogens in animal receiving combbined therapy were higher than those in respective controls.In conclusion,the results showed that appropriate administration of cytostatics and BRM may be beneficial in the treatment of liver metastasis. It is likely that splenic macrophages played a mayor role in controlling of tumor growth in the liver.

  14. Type of paper: Summary in proceedings

    Title: The effect of hyperbaric oxygen on the growth of the anaplastic carcinoma in Y59 rats lungs - cellular and humoral response

    Authors:
    Košuta-Špoljar, Dunja (81851)
    Arbanasić, Haidi
    Bašić, Ivan (2406)
    Editors
    Gomerčić, Hrvoje
    Proceedings title: Zbornik sažetaka priopćenja petog kongresa biologa Hrvatske s međunarodnim sudje
    Place: Zagreb
    Year: 1994
    ISBN/ISSN: 953-6241-01-3
    Pages: from 163 to 164
    Meeting: Peti kongres biologa Hrvatske s međunarodnim sudjelovanjem
    Held: from 10/03/94 to 10/07/94
    Summary: The effect of hyperbaric oxygen ( HBO ) on the growth of anaplastic carcinoma ( ACa ) colonies of lungs of Y59 rats observed. From the first day after i.v. tumor cell injection ( 2x104 ACa cells ) the animals were exsposed to hyperbaric oxygen ( 300 kPa ) during 18 days ( 90 min/day ). The number of colonies on the lung;s surface of the rats exsposed to HBOwas significantly smaller in number ( 4,2+-0,9 ) in comparison to control animals ( 44,3+-8,2 ). We have also found the weight of lungs to be significantly smaller ( 1,5+-0,09 g )in comparison with the control values ( 4,21+-0,05 g ). There has been found that 65% of rats exsposed to HBO didn;t have any macro- or micrometastases in their lungs. Mononuclear cells from experimental and control animals were purified on Ficoll Isopaque density gradient.Peripheral blood lymphocytes ( PBL ) ( 2x105 ) and splenocytes were stimulated with policlonal mitogens Phytohemagglutinin ( PHA ), Concanavalin A ( Con A ) and lypopolysacharide ( LPS ). Proliferation of PBL andsplenocytes was enhanced in those animals treated after ACa with HBO and showed significantly higher values in comparison to control animals ( given ACa cells ). However, reaction of HBO treated animals to mitogens was similar to normal healthy rats. Humoral immunological response was measured by plaque forming cells ( PFC ). Results showed that there is no significantly difference between experimental and control animals in different time intervals, except at day 20 after application of ACa cells in animals treated with HBO. These findings suggest that HBO may promote a new population of precursor cells to mitogenic responsive state and positive effect of HBO.

  15. Type of paper: Summary in proceedings

    Title: Royal jelly immunomodulation in rats and mice

    Authors:
    Šver, Lidija
    Oršolić, Nada
    Tadić, Zoran (143012)
    Valpotić, Ivica (66266)
    Bašić, Ivan (2406)
    Editors
    Gomerčić, Hrvoje
    Proceedings title: Zbornik sažetaka priopćenja petog kongresa biologa Hrvatske s međunarodnim sudje
    Place: Zagreb
    Year: 1994
    ISBN/ISSN: 953-6241-01-3
    Pages: from 212 to 213
    Meeting: Peti kongres biologa Hrvatske s međunarodnim sudjelovanjem
    Held: from 10/03/94 to 10/07/94
    Summary: In order to study possible immunomodulatory effect of royal jelly ( RJ ) secreted by mandibular and hypopharyngeal glands of worker honeybee ( Apis mellifera L. ) we have used well established rodent model. CBA mice received s.c. 0,1 ml of RJ ( Experiment 1 ), and Y59 rats were given i.m. 0,4 ml or i.v. 0,025 ml of RJ, respectively ( Experiment 2 ), by one or two injection in 7 day intervals. In mice which were immunized with 4x108 of SRBC 7 days after application of RJ the number of plaque forming splenocytes was significantly higher ( P<0,05 ) than that in nontreated controls. Both, weight inguinal lymph node and number of peripheral blood lymphocytes were increased ( P<0,05 ) in RJ- treated mice 3 or 5 days after immunization, respectively. Neutrophils were decreased ( P<0,05 ) in the mice that were killed 5 or 10 days after RJ treatment. Serum levels of total proteins and immunoglobulins in rats that received RJ two times within 2-week-period were significantly lowered ( P<0,05 ) as compared with nontreated animals. Observed immunomodulatory effect of RJ should be additionally tested in vitro using immunocompetent cells and purified active substance(s) isolated from RJ.

  16. Type of paper: Summary in proceedings

    Title: Antimetastatic activity of bee venom and water - soluble derivative of propolis in mice

    Authors:
    Bašić, Ivan (2406)
    Ćurić, Stipica (108013)
    Tadić, Zoran (143012)
    Oršolić, Nada
    Sulimanović, Đuro (45465)
    Editors
    Borneck, P.
    Stern, W.
    Cochard, Jean - Paul
    Proceedings title: 34th International Apicultural Congress - Programme and summaries of the reports
    Language: engleski
    Place: Bucharest, Romania
    Year: 1995
    Pages: from 135 to 136
    Meeting: 34th Congress Apimondia
    Held: from 08/15/95 to 08/19/95
    Summary: The effect of honeybee venom and water soluble propolis derivates ( WSD ) on tumor growth and metastasis formation in CBA mice was studied. Bee venom was injected into mice SC at doses of 0,15, 0,30, 0,60 mg/mouse and 0,15 or 0,075 mg/mouse SC or IV, respectively.WSD comprising 0,50 mg/kg of propolis was given IV. The tumor was a transpateble mammary carcinoma ( MCA ) weakly immunogenic to syngeneic CBA mice. Metastases were generated by injecting 1x103 MCA cells IV. The tumor in footpad was generated by 1x105 tumor cells. When tumor cells were injected into the footpad immediately after the bee venom, the growth of tumor was suppressed regardless of the dose of the venom. The survival of mice treated with 0,30 mg of bee venom was prolonged as compared to that of the control. Number of lung metastases in mice treated IV with 0,15 or 0,075 mg of bee venom was significantly lower ( P<0,001 ) comparing to that in nontreated mice. However, both doses of bee venom given SC did not reduce a number of lung metastases, indicanting that the antitumor effect of the venom couldbe highly depedent on the route of injection. WSD of propolis given to mice 7 days before IV administration of tumor cells significantly reduced the number of lung metastases. However, an injection of WSD o0f propolis given at the time of tumor cells injection or 7 days after had no effect on the number of metastases in the lung. The changes in several immunological parameters such as the response of lymphocytes to policlonal mitogens in vitro, production of tumor necrosis factors ( TNF- ) by lymphoid cells in vitro and rosette formation of lymphoid cells with SRBC, respectively corresponded positively with antimetastatic properties of both bee venom and WSD of propolis.
    Other: Poster PS 246 presented on 34th Congress of APIMONDIA: Z. Tadić, N. Oršolić, V. Lacković, S. Ćurić, I. Bašić: The effect of propolis on haematopoiesis (p. 64. in 34th Congress Apimondia Programme and summaries of the reports)

  17. Type of paper: Summary in proceedings

    Title: Atimetastatic efficacy of levamisole and 5 - FU as adjuvant to surgery of a rat colonic carcinoma

    Authors:
    Bašić, Ivan (2406)
    Kaštelan, Željko
    Eljuga, Damir (87925)
    Kaštelan, Maja
    Oršolić, Nada
    Tadić, Zoran (143012)
    Proceedings title: 16th International Cancer Congress 1994 - Abstract Book - I (Oral & Poster Prese
    Language: engleski
    Place: New Delhi, India
    Year: 1994
    Pages: from 305 to 305
    Meeting: 16th International Cancer Congress 1994
    Held: from 10/30/94 to 11/05/94
    Summary: The result of surgical removal of a large bowel tumor is of uncertain prognosis for a patient because of possible previous release of tumor cells from primary tumor into systemic and portal circulation. We have studied the effect of surgery combined with adjuvant therapy with levamisole and 5-FU on the development of liver metastases of a transpantable rat colonic carcinoma and the effect of such therapy on immunological status of rats, respectively. Tumor was generated by injection 5x103 tumor cells into the colon wall. Twenty one days after inoculation of tumor cells, the tumor was surgically removed and animals wetre allocated to the following regimes: (a) no treatment, (b) levamisole ( 4 mg/kg every 8 h during three postoperative days and then on days 14 and 21 ), (c) 5 -FU ( 10 mg/kg, same schedule as for levamisole ), and (d) the combination of levamisole and 5-FU at the same dose and schedule as above. Animals were checked for liver metastases 51 days after the initiation of the experiments. Significantly fewer adjuvant-treated animals had metastases than those undergoing surgery alone ( P<0,05-0,001 ). Combined treatment with both 5-FU and levamisole after surgery restored immunological reactivity of spleen cells ( NK, proportion of T and B lymphocytes, actyvity to mitogens ) which was deteriorated either by the presence of the tumor or by surgery and 5-FU treatment, respectively. In conclusion, adjuvant terapy with levamisole plus 5-FU suppressed the growth of metastases of colonic adenocarcinoma in the liver partially through the reparation of immune reaction.
    Keywords: colon, tumor metastasis, levamisole, 5 - FU
    Other: Sažetak se nalazi u knjizi pod brojem PSB12 - 07

  18. Type of paper: Summary in proceedings

    Title: Effect of locally administered cytostatic therapy and BRM on liver metastasis of a colon tumor in the rat

    Authors:
    Bašić, Ivan (2406)
    Kujundžić, Milan (168490)
    Kaštelan, Maja
    Oršolić, Nada
    Tadić, Zoran (143012)
    Ćurić, Stipica (108013)
    Šamija, Mirko (66200)
    Proceedings title: 16th International Cancer Congress 1994 - Abstract Book I - Oral & Poster Presen
    Language: engleski
    Place: New Delhi, India
    Year: 1994
    Pages: from 339 to 339
    Meeting: 16th International Cancer Congress 1994
    Held: from 10/30/94 to 11/05/94
    Summary: Using a model of artifical liver metastasis of a weakly immunogeneic colon adenocarcinoma of the rat, the antitumor effect of intrahepatally administered doxorubicin of 5 - FU combined with ip administration of the biological response modifiers (BRM), levamisole, IL - 2 or a lyophilized extracct of the plant Caucalis platycarpos L. was studied. Animals that received cytostatics alone survived significantly longer than untreated control; the increase of the dose resulted in better survival and the lesions to the bone marrow in these animals were not augumented. Complete disappearance of liver metastasis was frequently observed when the administration of cytotoxic drug was combined with either biological response modifier. In addition BR added to the drug therapy prevented the dissemination of tumor cells to the other organs. Immunological parameters such as NK activity and response to mitogens in animals treated with cytotoxic drugs and RM were elevated In conclusion, the results showed that appropriate administration of cytostatics together with BRM may be beneficial in the treatment of liver metastasis.
    Keywords: colon tumor, BRM, combined therapy
    Other: Sažetak je naveden u knjizi pod brojem PSB23 - 13

  19. Type of paper: Ph.D.

    Title: The effect of chemotherapy and immunomodulators on liver metastases of the colon adenocarcinoma in rats
    Faculty: Medicinski fakultet Sveučilište u Zagrebu
    Author: AGANOVIĆ IZET
    Language: hrvatski
    Number of pages: 127
    Summary: This study was conducted to investigate the effect of combinedchemoimmunotherapy on the colorectal carcinoma and livermetastases in rats. It has been demonstrated that intrahepaticadministration of daunorubicin and lipiodol as well asdoxorubicin, 5 - fluorouracil in combination with lipiodolresulted in significant improvement in the rate of survival amongexperimental animals and complete disappearance of liver tumors.The results of treatment without lipiodol administration were, tosome extent, inferior. Administration of 5 - fluorouracil alonedid not produce satisfactory results. the results of treatmentwith the above mentioned combined treatment modalities weresignificantly better if various immunomodulatory agents have beenadministered simultaneously. Namely, levamisole producedsignificant antitumor effect, as previously mentioned in theliterature. however, the new immunomodulator, plant extract namedCDL produced better results than levamisole. By using test oflymphocyte blast transformation by mitogens and NK activity assaywe showed that levamisole, IL - 2 and CDL increased T lymphocyteand NK cell activity. On the other hand, no detrimental effectson liver functions, hematological parameters and bone marrowcellularity were noted. In summary, we concluded that the abovementioned forms of chemoimmunotherapy did not produce seriousadverse effects, deserving great attention in furtherinvestigations and possible clinical applications.


  20. Type of paper: Ph.D.

    Title: The transforming and transactivating capability of the hepatitis b virus X gene
    Faculty: Prehrambeno - biotehnološki fakultet Sveučilište u Zagrebu
    Date of defense: 03/17/92
    Language: hrvatski
    Number of pages: 140
    Summary: In this series of experiments, the transforming andtransactivating potential of normal and mutated hepatitis B virusX gene was investigated. Transfection of Hep G2 cells with normaland mutated HBV genomes showed that gene X is not involved inviral replication but is responsible for DNA packaging andformation of viral particles. The transforming potential of the Xgenes was investigated using focus - forming assay on confluentmonolayers of NIH 3T3 cells and colony formation of NIH 3T3fibroblasts and BNL CV 2 cells in soft agar. In this assay, themutated HBV X gene showed greater transforming potential than itsnormal counterpart. Also, NIH 3T3 cells with mutated X geneformed more tumors in nude mice. The transactivating ability ofthe HBV X gene was assayed on the SV 40 early promoter. It wasshown that normal gene is potent transactivator while mutatedgene failed to activate transcription "in trans". Thetransactivating ability of normal HBV X gene is preserved inintegrated state in HuH - 7 cells. However, CAT assays withdifferent parts of HuH - 7 integrate confirmed the existence ofanother transactivator, presumably in the S region of the HBVgenome. The expression of the HBV X gene in retroviral vector(proviral expression) confirmed the results obtained usingplasmids the HBV X genes. On the basis of this experiments, anew, dual function of ORF X can be postulated. The first productof HBV X gene is strong transactivator but cannot transform cells"in vitro". The second product does not have transactivatingability but is capable of transforming NIH 3T3 and BNL CV 2cells.


  21. Type of paper: Mentorship

    Title: Induction of murine splenic tumoricidal macrophages by cytokines
    Faculty: Prirodoslovno - matematički fakultet Sveučilište u Zagrebu
    Mentor: BAŠIĆ IVAN
    Number of pages: 204
    Author: Verstovšek Dr. Srđan
    Degree level: Ph.D.



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