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Biomedical subjects

P I Liu

Publications and source records attributed to P I Liu.

At least 19 recordsLinked to original sources
PubMed1993

Mucous gland metaplasia of the prostate.

Mucous gland metaplasia of the prostate was observed in 11 of the 1,236 autopsy cases. The cells were characterized by plump cytoplasmic mucin and tiny nuclei that were basally oriented. They resembled Cowper's gland (bulbourethral gland) epithelium. The lesion was located randomly within the glands and was very small; only one was larger than 1 mm2. The cytoplasmic mucin was periodic-acid Schiff positive and immunohistochemically negative for prostate-specific antigen. Lectin binding profiles were different from those of normal prostatic glandular epithelium and also from those of Cowper's gland. The importance of recognizing mucous metaplasia lies in its differentiation from other lesions, especially from low-grade carcinoma.

Adult↗
PubMed1991

Pathological features of renal cell carcinoma incidentally discovered at autopsy.

Renal cell carcinomas incidentally discovered at autopsy (IRCs) were retrospectively analyzed to determine whether they had any pathological features differing from clinical renal cell carcinomas (CRCs): From 7,970 autopsy cases, there were 51 cases (0.65%) of renal cell carcinoma (RC) including 42 men and 9 women (ratio 4.6:1). The mean age of RC cases was 66.3 +/- 12.9 (range of 20 to 91 years). Of the 51 RC cases, approximately half of them (25/51) were IRC cases. No difference was shown in age and sex between IRC and CRC cases. Mean tumor size of IRC was 2.6 +/- 2.5 cm in diameter. This was significantly smaller (P less than 0.01) than that of CRC (7.3 +/- 2.8 cm). Histologically, both grade 1 and clear cell type were significantly more predominant among IRC cases than CRC cases (P less than 0.01 and P less than 0.05, respectively). Only one out of 25 cases of IRC had distant metastasis, as compared to 23 out of 26 CRC cases (88.5%). These pathological features indicate that the incidentally discovered renal cell carcinoma may have less malignant potential than clinical tumors. Unexpectedly, the majority of the IRC cases (88.0%) were associated with advanced neoplasia of other sites, as compared to only 19.0% of CRC cases (P less than 0.01).

Adult↗
PubMed1990

Differential expression of class I major histocompatibility complex determinants by lymphoblastic leukemia-lymphoma cell lines.

Two T-cell lines (XR11-4T and XR11-5T), established from radiation-induced, murine lymphoblastic lymphomas, were examined for the expression of class I major histocompatibility complex antigen and tumor induction. These cell lines expressed class I private determinants, H-2.9 and H-2.26, but not the monomorphic determinant defined by monoclonal antibody M1/42. Both cell lines produced tumors in syngeneic and allogeneic hosts. The monomorphic determinant could be demonstrated on both cell lines following growth in allogeneic (BALB/c mice) but not in syngeneic (RFM mice) hosts. The re-expressed determinant present on cells following growth in allogeneic mice was not of host origin. Thus, tumorigenic x irradiation may differentially affect the expression of class I major histocompatibility complex determinants.

Animals↗
PubMed1989

Adrenal myelolipoma: preoperative diagnosis by fine-needle aspiration cytology.

Fine-needle aspiration (FNA) was performed under ultrasonographic guidance on a suprarenal mass in a 52-yr-old Japanese man. Preoperatively, the diagnosis of adrenal myelolipoma was easily established from the cytologic findings of the aspirates. FNA is a very useful technique for the differential diagnosis of this tumor, and it is particularly valuable for many hospitals that are not equipped with computed tomography.

Adrenal Gland Neoplasms↗
PubMed1989

Bilateral diffuse nephroblastomatosis, pancortical type. A case report with immunohistochemical investigations.

A variation of Perlman's syndrome of the pancortical type is reported in a male neonate whose parents were cousins. The patient was the product of a 35-week pregnancy, the Apgar score was 3, and the patient died of respiratory failure one hour and 12 minutes after delivery. Autopsy revealed bilateral diffuse nephroblastomatosis, pancortical type, associated with malformations (usually facial), congenital anomalies of the heart, hepatosplenomegaly, pancreatic islet cell hyperplasia, bilateral cryptorchidism, and hyperflexibility of the left knee joint. Renal immunohistochemical investigations revealed positive bindings with peanut and soybean agglutinins and epithelial membrane antigen along the luminal surface of the epithelium in the moderately differentiated tubules, but not in blastoma or primitive epithelium.

Abnormalities, Multiple↗
PubMed1988

Human squamous cell carcinoma lines express oncofetal 44-kD polypeptide defined by monoclonal antibody to mouse fetus.

Most primary human carcinomas uniformly express an oncofetal epitope which has not been demonstrated previously in established human carcinoma cell lines. We successfully derived several low-passage cell lines of human squamous cell carcinoma (SCC) from head and neck tumors using an in vitro adaptation procedure, characterized these lines, and examined them for expression of a 44-kilodalton (kD) polypeptide (PP) oncofetal antigen (OFA) at the cell surface. Newly established an in vitro-passaged SCC cells retained characteristic microvilli, numerous desmosomes and tonofilaments, abundant rough endoplasmic reticulum, osmophilic keratohyaline granules, and other features of the primary SCC cells. These new cell lines and two long-term, established SCC lines (FaDu and Detroit 562) displayed OFA at the cell surface, as determined by flow cytometry using monoclonal antibody (MoAb) 115. While the FaDu and Detroit 562 lines exhibited aneuploidy during flow cytometric analysis, the new, low-passage SCC lines that we developed remained diploid as were the primary SCC cells from which they were derived. We propose that the expression of a 44-kD OFA is a common feature of human SCC. This marker may prove useful in the detection and treatment of these tumors.

Antibodies, Monoclonal↗
PubMed1988

Radiation-induced lymphoblastic lymphomas/leukemias and sarcomas of mice express conserved, immunogenic 44-kilodalton oncofetal antigen.

X-ray-induced, lymphoblastic, T-cell lymphoma/leukemias from irradiated RF mice were observed to uniformly expressed a 44-kd oncofetal antigen (OFA). The OFA polypeptide was detected by flow cytometry, affinity column SDS-PAGE analysis, and immunoblotting with monoclonal antibody (MAb) 115 prepared against syngeneic mouse fetus. X-ray and ultraviolet (UV) induced murine fibrosarcoma cell lines, used as classic models in radiation biology, were also found to express the OFA, which suggested that the 44-kd OFA was a general transformation marker of tumors. Adult mouse thymocytes and other adult tissues expressed no OFA. The 44-kd polypeptide was located at the surface membrane of the tumors examined. In contrast to other reports, lymphoblastic lymphoma cell lines expressed the OFA as a cross-protective, rather than an individually-specific, tumor-associated transplantation antigen. Pronase treatment removed OFA from the surface of living lymphoma cells, whereas collagenase, neuraminidase, and hyaluronidase did not. The OFA was rapidly reexpressed upon culture of the pronase-treated cells. Taken together, these results suggest that the 44-kd OFA polypeptide described here may provide a useful cell surface marker for future radiation carcinogenesis studies. MAb 115 is a promising reagent for detecting tumor-associated 44-kd OFA, for assessing immunoregulatory perturbations to the OFA caused by radiation damage and for investigating the immunopathology of OFA-associated radiation damage.

Animals↗
PubMed1986

A rapid assessment of percentage hemoglobin-S in whole blood.

In an effort to bridge the gap between the rapid Sickledex screening test (Ortho Diagnostics, Raritan, NJ) and the slow but quantitative hemoglobin electrophoresis, the authors developed a rapid method for quantification of the percentage of hemoglobin S (%Hgb-S) in whole blood. The method involves quantification of the hemoglobin before and after removal of sodium dithionite-induced sickled cells for calculation of the %Hgb-S. Test results were within a +10% range of hemoglobin electrophoresis, with 67% of results within a +5% range. The method, taking 30-45 minutes to perform, offers a rapid assessment of %Hgb-S in acute care situations.

Hemoglobin, Sickle↗