Inhibition of pulmonary metastases and tumor cell invasion in experimental tumors by sodium D-glucaro-delta-lactam (ND2001)
- PMID: 7737908
- PMCID: PMC5920576
- DOI: 10.1111/j.1349-7006.1995.tb02986.x
Inhibition of pulmonary metastases and tumor cell invasion in experimental tumors by sodium D-glucaro-delta-lactam (ND2001)
Abstract
Sodium D-glucaro-delta-lactam (ND2001) inhibited spontaneous pulmonary metastases of the highly metastatic B16 melanoma variant with a maximal inhibition rate of 99.5%, and 6 of 7 animals remained metastasis-free. Likewise, ND2001 inhibited the spontaneous pulmonary metastases of both Lewis lung carcinoma (3LL) with a rate of 98.0% (3 of 5 animals remaining metastasis-free) and rat KDH-8 liver carcinoma with a rate of 82.5% (3 of 7 animals remaining metastasis-free), although it was unable to inhibit the metastases of mouse BMT-11 fibrosarcoma and rat SST-2 breast carcinoma. Pretreatment with ND2001 in vitro inhibited the pulmonary metastases of the B16 variant and 3LL cells, which indicates direct action upon the cancer cells. When the invasive activity of cancer cells was measured by the Boyden chamber method, the number of invading B16 variant or 3LL cells was reduced with maximal inhibition rates of 93.0% or 89.9%, respectively, but pretreatment with ND2001 failed to reduce the invasive activity of BMT-11 or SST-2 cells. ND2001 showed neither cytocidal nor antitumor activity. These results suggest that ND2001 inhibited pulmonary metastases at the invasive step into the basement membrane by directly changing some property of the tumor cells.
Similar articles
-
Inhibition of tumor cell haptotaxis by sodium D-glucaro-delta-lactam (ND2001).Jpn J Cancer Res. 1995 Nov;86(11):1080-5. doi: 10.1111/j.1349-7006.1995.tb03024.x. Jpn J Cancer Res. 1995. PMID: 8567400 Free PMC article.
-
Inhibition of liver metastases and tumor cell invasion in spontaneous liver metastasis model (LMFS) by sodium D-glucaro-delta-lactam (ND2001).Biomed Pharmacother. 2000 Mar;54(2):85-92. doi: 10.1016/S0753-3322(00)88857-5. Biomed Pharmacother. 2000. PMID: 10759292
-
Inhibitory effect of ND2001 on spontaneous multiple metastasis of NC 65 tumors derived from human renal cancer cells intradermally transplanted into nude mice.Anticancer Drugs. 1999 Feb;10(2):229-33. doi: 10.1097/00001813-199902000-00012. Anticancer Drugs. 1999. PMID: 10211554
-
gem-Diamine 1-N-iminosugars and related iminosugars, candidate of therapeutic agents for tumor metastasis.Curr Top Med Chem. 2003;3(5):575-91. doi: 10.2174/1568026033452492. Curr Top Med Chem. 2003. PMID: 12570867 Review.
-
Potential use of D-glucaric acid derivatives in cancer prevention.Cancer Lett. 1990 Oct 8;54(1-2):1-8. doi: 10.1016/0304-3835(90)90083-a. Cancer Lett. 1990. PMID: 2208084 Review.
Cited by
-
Inhibition of tumor cell haptotaxis by sodium D-glucaro-delta-lactam (ND2001).Jpn J Cancer Res. 1995 Nov;86(11):1080-5. doi: 10.1111/j.1349-7006.1995.tb03024.x. Jpn J Cancer Res. 1995. PMID: 8567400 Free PMC article.
References
-
- ) Fidler , I. J.General considerations for studies of experimental cancer metastasis . Methods Cancer Res. , 15 , 399 – 439 ( 1978. ).
-
- ) Liotta , L. A.Tumor invasion and metastases — role of the extracellular matrix: Rhoads memorial award lecture . Cancer Res. , 46 , 1 – 7 ( 1986. ). - PubMed
-
- ) Tsuruoka , T. , Fukuyasu , H. , Azetaka , M. , Iizuka , Y. , Kawaharajo , K. , Inouye , S. , Hosokawa , M. and Kobayashi , H.Inhibition of pulmonary metastases in experimental tumors by d‐glucaro‐δ‐lactam sodium salt (ND2001) . Abstr. 2nd Joint Meet. AACR/JCA. No. B‐3 ( 1992. ).
-
- ) Tsuruoka , T. , Niwa , T. , Shomura , T. , Matsuno , T. , Itoh , N. , Inouye , S. and Niida , T.Synthesis of d‐glucaro‐δ‐lactam, an oxidation product of Nojirimycin . Sci. Rep. Meiji Seika Kaisha , 13 , 80 – 84 ( 1973. ).
-
- ) Ishikawa , M. , Hosokawa , M. , Oh‐hara , N. , Niho , Y. and Kobayashi , H.Marked granulocytosis in C57BL/6 mice bearing a transplanted BMT‐11 fibrosarcoma . J. Natl. Cancer Inst. , 78 , 567 – 571 ( 1987. ). - PubMed
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical