TY - JOUR
T1 - Effect of tumor removal on the presence of lymphocytic cortisol metabolism-enhancing factor in plasma of cancer patients
AU - Barkan, Ariel
AU - Spalter, Henriette Hoogervorst
AU - Kaufman, Haiuta
AU - Klein, Ami
N1 - Funding Information:
1 Received September 6. 1979; accepted December 2, 1979. 2 Supported by The Israel Cancer Research Fund (George and Rose Blumenthal Research Fellowship for Hodgkin's Disease). 3 Research procedures were in accord with the ethical 3tandards of the Helsinki Declaration of 1975. 4 Medicine "B" Department, Beilinson Medical Center, Petah-Tiqva. Israel. , Endocrinological Laboratory, Beilinson Medical Center. 6 Address reprint requests to Dr. Klein. 1 We are grateful to Dr. J. Malchi and his staff, Beilinson Hospital Blood Bank. for supplying buffy coats. We also thank Mrs. R. Fradkin for revising the manuscript.
PY - 1980/6
Y1 - 1980/6
N2 - Because lymphocytic cortisol metabolism-enhanc- ing factor (LCMEF) Is absent In the plasma of cancer patients (CP), this study was undertaken to determine the Influence of tumor removal on this phenomenon. Known concentrations of human lymphocytes were incubated with cortisol in media con-taining 50% phosphate-buffered saline (PBS) and 50% of one of the following: A) homologic normal plasma (HP), b) plasma from patients with noncancerous diseases (NCD) before surgery, c) plasma from patients with NCD after surgery, d) plasma from CP before tumor removal, e) plasma from CP after tumor removal, f)plasma from long-surviving CP (LSCP), and g) PBS. With the exception of plasma from the LSCP group, all the plasma had the capacity to enhance the lymphocytic cortisol metabolism (LCM) when compared with that of PBS. There was no significant difference between the metabolism obtained with HP and that obtained with plasma from patients with NCD either before or after surgery. The plasma from CP led to a significant reduction In activity, with no significant difference in conversion rates before and after tumor removal. The plasma from LSCP failed to enhance LCM, had a conversion rate similar to that of PBS and significantly lower than that of the plasma from CP, and appeared to contain no LCMEF. These findings, which showed that the lack of LCMEF in CP is not Influenced by tumor removal, may indicate 1) that the lack of LCMEF preceded the appearance of cancer or 2) irreversibility of a possible antl-LCMEF synthesis effect waS induced by the tumor.
AB - Because lymphocytic cortisol metabolism-enhanc- ing factor (LCMEF) Is absent In the plasma of cancer patients (CP), this study was undertaken to determine the Influence of tumor removal on this phenomenon. Known concentrations of human lymphocytes were incubated with cortisol in media con-taining 50% phosphate-buffered saline (PBS) and 50% of one of the following: A) homologic normal plasma (HP), b) plasma from patients with noncancerous diseases (NCD) before surgery, c) plasma from patients with NCD after surgery, d) plasma from CP before tumor removal, e) plasma from CP after tumor removal, f)plasma from long-surviving CP (LSCP), and g) PBS. With the exception of plasma from the LSCP group, all the plasma had the capacity to enhance the lymphocytic cortisol metabolism (LCM) when compared with that of PBS. There was no significant difference between the metabolism obtained with HP and that obtained with plasma from patients with NCD either before or after surgery. The plasma from CP led to a significant reduction In activity, with no significant difference in conversion rates before and after tumor removal. The plasma from LSCP failed to enhance LCM, had a conversion rate similar to that of PBS and significantly lower than that of the plasma from CP, and appeared to contain no LCMEF. These findings, which showed that the lack of LCMEF in CP is not Influenced by tumor removal, may indicate 1) that the lack of LCMEF preceded the appearance of cancer or 2) irreversibility of a possible antl-LCMEF synthesis effect waS induced by the tumor.
UR - http://www.scopus.com/inward/record.url?scp=0018883733&partnerID=8YFLogxK
U2 - 10.1093/jnci/64.6.1333
DO - 10.1093/jnci/64.6.1333
M3 - מאמר
AN - SCOPUS:0018883733
VL - 64
SP - 1333
EP - 1335
JO - Journal of the National Cancer Institute
JF - Journal of the National Cancer Institute
SN - 0027-8874
IS - 6
ER -