Detection of tumor specific gene expression in bone marrow and peripheral blood from patients with small cell lung carcinoma
✍ Scribed by Masato Shingyoji; Yuichi Takiguchi; Reiko Watanabe; Kenzo Hiroshima; Ken Motoori; Katsushi Kurosu; Yasunori Kasahara; Nobuhiro Tanabe; Koichiro Tatsumi; Takayuki Kuriyama
- Publisher
- John Wiley and Sons
- Year
- 2003
- Tongue
- English
- Weight
- 84 KB
- Volume
- 97
- Category
- Article
- ISSN
- 0008-543X
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
BACKGROUND
Small cell lung carcinoma (SCLC) has the propensity to grow rapidly and metastasize extensively. Detection of micro‐dissemination of SCLC may have clinical relevance. For its detection, tumor‐specific gene expressions were examined in peripheral blood and bone marrow aspirate from patients with SCLC.
METHODS
Expression of prepro‐gastrin‐releasing peptide (preproGRP), neuromedin B receptor (NMB‐R) and gastrin‐releasing peptide receptor (GRP‐R) were examined by reverse transcriptase polymerase chain reaction (RT‐PCR) in peripheral blood and bone marrow aspirate from 40 untreated patients with SCLC. Control samples consisted of peripheral blood samples from 5 patients with nonsmall cell lung cancer (NSCLC) and 20 healthy volunteers.
RESULTS
Positive rates of preproGRP, NMB‐R, and GRP‐R in bone marrow aspirate of patients with SCLC were 23% (9/40), 8% (3/40), and 10% (4/40), respectively. Those rates in peripheral blood were 11% (4/38), 5% (2/38), and 29% (11/38), respectively. Although GRP‐R expression was detected in patients with NSCLC and in healthy volunteers, preproGRP and NMB‐R expressions were not detected in patients with NSCLC and in healthy volunteers. All three gene expressions in bone marrow were more frequently observed in patients with bone marrow metastasis, accessed by biopsy, than in patients without. PreproGRP gene expression in bone marrow was also more frequent in patients with bone metastasis, accessed by bone scintigram, than in patients without, and was related to poorer survival.
CONCLUSIONS
Micro‐dissemination of SCLC was detectable by RT‐PCR of preproGRP and NMB‐R, both specific for SCLC. These gene expressions in bone marrow may be related to disease extent and prognosis. Cancer 2003;97:1057–62. © 2003 American Cancer Society.
DOI 10.1002/cncr.11108
📜 SIMILAR VOLUMES
## Background: Several sensitive surveillance tests reportedly have been used to detect occult neuroblastoma (nb) cells in peripheral blood (pb) and bone marrow (bm). they may be useful in monitoring minimal residual tumor cells. the authors report the feasibility and clinical usefulness of a sensi
## Abstract Bone marrow (BM) is accepted as the tissue of choice for the detection of monoclonal populations in leukemias and lymphomas; however, obtaining BM can be painful and traumatic for the patients. Although it is possible to detect clonality in peripheral blood (PB) samples, there are no re
Non-small-cell lung cancers (NSCLC) are often infiltrated by T lymphocytes. It is postulated that the presence of tumor-infiltrating lymphocytes (TIL) reflects a local host immune response against autologous tumors. To identify the nature of NSCLC TIL, we have characterized the molecular structure o