HER-2/ neu and CD117 (c-kit) overexpression in patients with pesticide exposure and extensive stage small cell lung carcinoma (ESSCLC)
Anil Potti1, Apar Kishor Ganti2, Sascha A Tuchman3, Kaley Sholes4, Eric Langness4, Vijay Koka4, Michael Koch5
1 Department of Medicine, Divisions of Hematology and Oncology, Duke University Medical Center, Durham, NC 27715, USA
2 Department of Medicine, Section of Oncology-Hematology, University of Nebraska Medical Center, Omaha, NE 68198-7680, USA
3 Department of Medicine, Duke University Medical Center, Durham, NC 27715, USA
4 Department of Medicine, University of North Dakota School of Medicine, Fargo, ND 58102, USA
5 Department of Pathology, Meritcare Medical Center, University of North Dakota School of Medicine, Fargo, ND 58122, USA
|Date of Submission||30-Aug-2004|
|Date of Acceptance||09-Jun-2005|
|Date of Web Publication||09-Jun-2005|
Department of Medicine, Divisions of Hematology and Oncology, Duke University Medical Center, Durham, NC 27715
Source of Support: None, Conflict of Interest: None
Background: The rate of detection of HER-2/ neu and CD117 (c-kit) overexpression in small cell lung cancer (SCLC) has varied widely; between 5-35% and 21-70% respectively.
Methods: To evaluate the relationship between pesticide exposure and HER-2/ neu and CD117 overexpression in extensive stage SCLC (ESSCLC), we identified patients with ESSCLC and assessed pesticide exposure using a predetermined questionnaire. An exposure index (hours/day × days/year × years) ≥ 2400 hours was considered as 'exposed.' HER-2/ neu overexpression was evaluated on archival tissue using the DAKO Hercep test, and CD117 testing was performed using immunohistochemistry (A4052 polyclonal antibody).
Results: 193 ESSCLC patients were identified. Pesticide exposure data could be obtained on 174 patients (84 females and 109 males) with a mean age of 68.5 years. 53/174 (30.4%) revealed HER-2/ neu overexpression. 54/174 (31.03%) specimens showed CD117 overexpression by IHC. On multivariate analysis, HER-2/ neu overexpression was associated with diminished survival (p < 0.001). In comparison, CD117 expression did not have an adverse prognostic value (p = 0.025). 41/53 (77.4%) patients with HER-2/ neu overexpression and 47/121 (38.8%) patients without overexpression had exposure to pesticides (odds ratio: 5.38; p < 0.01). Among the cohort tested for CD117, 29/54 (53.7%) patients with CD117 overexpression and 59/120 (49.2%) patients without CD117 overexpression had pesticide exposure (odds ratio: 1.18; p = 0.12).
Conclusion: Pesticide exposure affects HER-2/ neu but not CD117 overexpression. Future studies are needed to determine specific pesticide(s)/pesticide components that are responsible for HER-2/ neu overexpression in ESSCLC, and to validate our findings in other solid tumors that overexpress HER-2/ neu .
|How to cite this article:|
Potti A, Ganti AK, Tuchman SA, Sholes K, Langness E, Koka V, Koch M. HER-2/ neu and CD117 (c-kit) overexpression in patients with pesticide exposure and extensive stage small cell lung carcinoma (ESSCLC). J Carcinog 2005;4:8
|How to cite this URL:|
Potti A, Ganti AK, Tuchman SA, Sholes K, Langness E, Koka V, Koch M. HER-2/ neu and CD117 (c-kit) overexpression in patients with pesticide exposure and extensive stage small cell lung carcinoma (ESSCLC). J Carcinog [serial online] 2005 [cited 2017 Aug 18];4:8. Available from: http://www.carcinogenesis.com/text.asp?2005/4/1/8/42213
| Introduction|| |
Lung cancer is the most common malignancy both in terms of incidence and mortality in the world. In 1999, there were 1.04 million new cases (12.8%) and 921,000 deaths (17.8%) due to lung cancer all over the world . It is expected that in 2004, there will be 173,770 new cases of lung cancer diagnosed and 160,440 people will die of lung cancer in the United States . Small cell lung carcinoma (SCLC), which comprises of 20% of lung cancer, is characterized by a rapid growth rate and early metastases [3,4]. Despite recent advances in therapy, the 2-year survival in limited stage small cell lung cancer is only 20-30% , while the median survival in extensive stage small cell lung cancer (ESSCLC) is less than a year (10.1 months) . Given these dismal survival rates, it is imperative that factors like biomarker profiles be evaluated in an attempt to define survival characteristics.
We had previously described the overexpression of HER-2/ neu in approximately 29% of patients with ESSCLC. In that same study, we also showed that this overexpression led to a poorer outcome . Micke et al found a definite amplification of c-erbB-2 oncogene in 13% of patients with SCLC; predominantly in ESSCLC. They thereby suggested that HER-2/ neu overexpression was more important in advanced stages of the disease . In contrast, however, Schneider and associates found minimal or no overexpression of HER-2/ neu in four out of four cell lines derived from small cell lung cancer . Similarly, Bunn et al evaluated eleven small cell lung cancer cell lines and found no evidence of HER-2/ neu overexpression .
In trying to explain these differences, we had hypothesized in our previous report that the difference in the methods used to detect HER-2/neu status (immunohistochemistry vs. fluorescent in situ hybridization) and the population studied (exclusively ESSCLC in our study), could have been responsible for the difference found in overexpression . However, we were unable to definitively explain the possible mechanisms responsible for this high rate of HER-2/ neu overexpression seen in our study.
We have also demonstrated earlier that CD117 (c-kit) overexpression occurred in about a third of patients with ESSCLC . The proto-oncogene c-kit encodes a transmembrane tyrosine kinase receptor (c-KIT/CD117) related to the platelet-derived growth factor (PDGF)/colony-stimulating factor-1 (CSF-1) (c-fms) receptor subfamily . CD117 is thought to play an important role in hematopoiesis, spermatogenesis, melanogenesis and, more recently, in carcinogenesis [12-14]. Overexpression of CD117 has previously been documented in myeloid leukemia, neuroblastoma, breast tumor, colon tumors, gynecological tumors, testicular germ cell tumors and SCLC [15-18].
Presented with two potential targets for therapy and/or possible predictors of survival, the objective for our current work was to undertake a retrospective comparison of the degree of overexpression of HER-2/ neu and CD117 in ESSCLC samples, with a possible link to prior pesticide exposure in our largely rural study population.
| Materials and methods|| |
After approval from the Institutional Review Board and the Human Subjects Committee, a two-phase retrospective study was performed. The records of all patients with a diagnosis of SCLC from January 1991 through April 2001 were reviewed. The data collected included the following variables regarding the patient's cancer history: age, sex, socioeconomic status, family history of cancer (if positive, type of cancer), smoking, performance score (ECOG), stage of cancer, treatment modality/modalities for SCLC, metastatic sites (other organs) involved, recurrent disease: symptoms at first recurrence age of recurrence, months from initial diagnosis and stage of disease at recurrence, treatment received for the recurrence, cause of death, other co-morbidities (non-malignant illnesses) and associated malignancies (if any) in the same patient. In addition, we conducted a population-based epidemiologic study in an effort to establish a relationship, if any, between pesticide exposure, ESSCLC and HER-2/ neu or CD117 overexpression.
Pesticide risk assessment interviews were performed (by a single member of the team for consistency) via telephone on the basis of a pre-determined questionnaire. The questionnaire investigated occupations and hobbies with special emphasis on:
(a) nature of exposure: insecticides and herbicides, organic solvents (paints, varnishes, solvents and glues) and petroleum products (diesels, petrol, oils, greases, dyes, inks and colorings),
(b) type of exposure (preparation and/or spraying of pesticide solutions, direct handling of solvents containing materials or petroleum products),
(c) use of protective measures in the workplace (dissolving or spraying the pesticide with pressurized containers, using glues or varnishes with adequate ventilation, etc.). The subject was considered as 'non-exposed,' in the presence of these effective protection measures.
(d) duration of exposure. An exposure index was calculated for each interviewed subject according to the following formula: hours/day × days/year × years . Patients with an exposure index >2400 h were considered as 'exposed', since previous reports have indicated that this figure represents heavy exposure to genotoxic agents [20,21].
HER-2/ neu oncoprotein overexpression was assessed by immunohistochemistry (IHC). Adequate pathologic samples were available on 193 subjects. IHC staining was carried out on formalin fixed, paraffin-embedded material, using the Hercep test developed by DAKO® Immunostaining was classified as follows: 0 = no staining; 1+ = faint, incomplete membranous pattern; 2+ = moderate, complete membranous pattern; 3+ = strong membranous pattern . A trained pathologist (M.K.), who was blinded from the clinical and exposure history of the patient, interpreted the IHC results. An IHC score of 2+ or greater was considered as positive for HER-2/ neu overexpression [23,24].
Detection of CD117 overexpression was assayed using an IHC technique on archival paraffin-embedded tissue specimens. Results were recorded on a semi-quantitative scale to record the number of positive cells (10%, 10-50% and >50%) and the intensity of reaction. CD117 status was reported as positive if it was >10% and negative if it was <10%. Immunohistochemical staining for c-kit (CD117) was performed using a 1:250 dilution of the rabbit polyclonal antibody A4502 (IMPATH, Los Angeles, CA, USA) with the EnVision detection system (IMPATH). An antigen retrieval method was not utilized. Appropriate positive and negative controls were used throughout the testing process. We used the A4502 antibody because it has shown consistent performance with a low background, because it seems to be the most widely used c-kit antibody, and because it is the antibody specified for CD117 testing in the large cooperative clinical trials of selective tyrosine kinase inhibitor STI-571. All interpretation of CD117 testing was performed by a single pathologist (M.K.) who was blinded from the clinical data of patients in our study population.
Statistical analysis was carried out using the chi-square test to evaluate the association between pesticide exposure and HER-2/ neu vs. CD117 overexpression, and the Mann Whitney U test to assess the impact of HER-2/ neu and CD117 overexpression on survival. Overall survival was calculated from the date of diagnosis of lung carcinoma by the Kaplan-Meier product limit method . Logistic regression analysis was performed to estimate the magnitude of the effect of pesticide exposure on HER-2/ neu and CD117 status. A multivariate analysis was performed to analyze the prognostic impact of overexpression of either oncoproteins. Statistical analysis was performed using SPSS-10®
| Results|| |
Between 1991 and 2001, 223 patients with ESSCLC were identified of whom 209 patients had complete records of treatment. The most common chemotherapeutic regimen involved using either cisplatin/carboplatin and etoposide or carboplatin and paclitaxel. The most common second-line agent used was docetaxel. 174 patients (98 males, 76 females) with a mean age of 68.5 years (range: 42-90 years) had adequate pathological specimens available for definitive HER-2/ neu and CD117 testing by IHC. The major symptoms at presentation and other relevant demographic data of the study population are described in [Table 1]. In our study, weight loss (52.8%) and cough (59.0%) were the two most common presenting complaints that showed a trend towards a decreased survival (p = 0.03) in patients with ESSCLC.
Fifty-three (30.4%) of the 174 specimens revealed HER-2/ neu overexpression by IHC while the remaining 121 (69.6%) did not [Table 1]. After adjusting for age, smoking, ECOG score and treatment, HER-2/ neu overexpression was associated with a statistically significant diminished survival (p < 0.001) . Of the 53 patients with HER-2/ neu overexpression, we were able to ascertain pesticide exposure in 41 patients (77.4%), while of the 121 without HER-2/ neu overexpression, 47 (38.8%) had a history of significant pesticide exposure, a statistically significant difference (odds ratio: 5.38; p < 0.01, 95% CI: 2.5 - 11.2). After adjusting for age, gender and smoking history, the odds ratio for developing a HER-2/neu positive tumor following pesticide exposure was still significant (odds ratio: 15.7; 95% CI 5.3 - 46.6; p < 0.01). The pesticide exposure occurred any time between 2 and 21 years prior to the diagnosis of the lung cancer. Patients with an exposure index >2400 h were considered as exposed although the length of exposure varied from 2400 to 7100 hrs.
As for CD117, of the 174 available specimens for review, 54 of 174 (31.0%) demonstrated IHC-verifiable CD117 overexpression, whereas 120 (69.0%) did not. Twenty-nine of the 54 patients overexpressing CD117 (53.7%) had evidence of pesticide exposure, whereas 59 of the 120 patients devoid of CD117 overexpression (49.2%) also had pesticide exposure (odds ratio 1.18; p = 0.12) [Figure 1]. Moreover, in contrast to HER-2/ neu , CD117 overexpression carried with it no adverse prognostic significance (p = 0.025).
| Discussion|| |
HER-2/ neu (also known as c- erb B-2) oncogene is the second member of the epidermal growth factor receptor family. It is overexpressed in many different types of human malignancies, notably, breast, lung, ovarian, gastric, pancreatic, colorectal, and cancers of the female genital tract [26-33]. HER-2/ neu overexpression seems to induce chemoresistance in certain experimental conditions. Also, HER-2/ neu overexpression has been associated with a poor overall survival and the development of metastatic phenotypes . These findings suggest that HER-2/ neu may serve as an excellent target for developing targeted anticancer agents, and indeed, the benefit of the monoclonal antibody against HER-2/ neu (trastuzumab) has been demonstrated in the treatment of metastatic breast carcinoma .
CD117 (c-kit) is a receptor-tyrosine kinase involved in regulation of hematopoiesis as well as cell migration of germ cells. Mutations in several key exons give rise to constitutive activation of the receptor that ultimately is responsible for the carcinogenesis of gastrointestinal stromal tumors. This finding has in part led to the creation of novel, tailored molecular therapy in the form of imatinib mesylate (STI571) that has been successful where many other anti-cancer therapies have failed .
Although animal studies demonstrate that many pesticides are carcinogenic, (e.g., organochlorines, creosote, and sulfallate) while others (notably, the organochlorines DDT, chlordane, and lindane) are tumor promoters, human data, however, are limited by the small number of studies that evaluate individual pesticides . In a case control conducted to evaluate the hypothesis that past exposure to the pesticide lead arsenate led to an excess mortality from respiratory cancer, Wicklund et al found that the presence, the intensity, nor the duration of exposure to lead arsenate differed between cases and control subjects . McDuffie et al reported an absence of correlation of lung cancer risk with occupational exposure to any specific pesticide or pesticides grouped by chemical composition . In contrast, Blair et al studied the mortality experience of a cohort of 3,827 white men licensed to apply pesticides in Florida to investigate health effects associated with chronic exposure to pesticides. They found an increasing risk of lung cancer with number of years licensed suggesting that some pesticides may be carcinogenic in humans . Similarly, De Stefani et al found that workers employed in the construction industry, as well as those exposed to DDT may have an excess risk of lung cancer . Becher and associates also showed an increased overall cancer mortality and mortality of respiratory cancer after long-term exposure to phenoxy herbicides and dioxins . Pesatori and co-workers showed that the risk of lung cancer was greater among those who worked as pest control operators than non-pest control workers .
In a predominantly agricultural state like North Dakota, where farming is the main occupation, exposure to various pesticides and herbicides is an everyday occurrence. Tessier and Matsumara have shown that in the human prostate cancer cell lines LNCaP and PC-3, erbB-2 kinase was activated by pesticides of different chemical classes: the organochlorine insecticides beta-hexa-chlorocyclohexane (beta-HCH), o,p'-dichlorodiphenyltrichloroethane (o,p'-DDT), heptachlor epoxide, the pyrethroid insecticide trans-permethrin, and the fungicide chlorothalonil . Similarly, in another study, Enan and Matsumara examined the effect of o,p'-DDT, the most estrogenic congener of the DDT family of chemicals and beta-HCH on protein phosphorylation activities in MCF-7, a line derived from human breast cancer cells. They found that o,p'-DDT activated c-neu (HER-2/ neu product protein) at extremely low concentrations . In a previous report, we had shown that pesticide exposure was associated with HER-2/neu overexpression .
With regards to CD117 overexpression, our prior work has demonstrated that CD117 is overexpressed in about 30% of patients with ESSCLC . Although the techniques to ascertain CD117 testing were different, since our reported prevalence of CD117 overexpression was different from that described in previous studies [46,47], and the fact that our study population was predominantly rural and mostly consisted on of the farming community, we decided to explore the link between CD117 overexpression and pesticide exposure. In addition, despite the evidence on the role of pesticides in the pathogenesis of lung cancer via potential avenues such as HER-2/ neu , the exact molecular role of pesticides on tumorigenesis in humans is unclear at this time.
Although there are no studies in lung cancer, either in patients or on cell lines demonstrating the biologic effects of pesticides or their components, our results indicate that pesticide exposure may indeed be related to HER-2/ neu but not CD117 overexpression in our select population with ESSCLC. We found that patients with HER-2/ neu overexpression were significantly more likely to have been exposed to pesticides (41/53; 77.4%), than those without HER-2/ neu overexpression (47/121; 38.8%) (Odds ratio: 5.38; p < 0.01). Our findings seem to agree with the field cancerization theory of Gazdar which states that all or much of the aerodigestive tract epithelium has been mutagenized, perhaps as the result of exposure to carcinogens leading to multiple molecular changes in individual cells ultimately resulting in carcinogenesis . Although there is a relative dearth of clinical studies, experimental studies using cancer cell lines revealed that HER-2/ neu was activated by various insecticides and fungicides of different chemical classes [43,44]. However, whether this activation translates into clinical malignancy has not been studied thus far. Our data suggest that the findings of these experimental models may in fact be true in the carcinogenesis of small cell lung cancer. Interestingly, however, CD117 overexpression was not more prevalent in patients with pesticide exposure (29/54; 53.7%) than those lacking such exposure (59/120; 49.2%) (Odds ratio 1.18, p = 0.12).
Thus, the difference in our reported prevalence of CD117 overexpression in ESSCLC and previous studies possibly was not due to pesticide exposure. Hibi et al.  reported that over 60% of cases with SCLC overexpress CD117. In another series, Sekido et al.  reported a higher incidence of CD117 overexpression (81%) in SCLC. The reason for the difference in our findings and the previous reports may be attributable to the fact that our large study included only patients with ESSCLC. Although the presence of CD117 does not carry definite prognostic value, it is possible that overexpression may be preferentially observed in patients with limited-stage SCLC. Earlier reports used northern or western blotting techniques for assessing CD117 expression; both of which are more sensitive but less specific than IHC techniques [49,50]. This difference in methodologies may also contribute to the observed difference in CD117 overexpression.
We realize that as with most questionnaire-based studies, a drawback of our study-design is the distinct possibility of a recall bias among the case population. In addition, in cases where the patient was deceased, the data was obtained from the next of kin, who may or may not have had detailed knowledge regarding pesticide exposure of the subject in question. Interviewing technique plays a central role in improving accuracy of the recall and is under the control of the investigator . We tried to minimize the effect of interviewing technique on the results by having one single investigator conduct all the interviews. Also, we used prompted questions, rather than open-ended question during the collection of exposure-data as that has been shown to decrease recall bias . Finally, another potential drawback to our study was the fact that although we gathered enough data regarding the extent of pesticide (insecticide/herbicide) exposure, while implementing our questionnaire, we failed to investigate the extent of exposure to specific pesticides/their components. However, it is possible that the effect of individual pesticides/pesticide components on HER-2/ neu overexpression may be better evaluated initially using SCLC cell lines .
In conclusion, HER-2/ neu overexpression was seen in slightly less than a third of patients with ESSCLC, and was associated with decreased survival. Conversely, CD117 overexpression was noted in approximately half of ESSCLC patients, but was not correlated to prognosis. Our data also suggest that pesticide exposure seems to be related to HER-2/ neu overexpression and may explain the increased incidence of overexpression detected in our study population. However CD117 expression appears to be uninfluenced by pesticides, at least at the level of exposure analyzed in our data. Future epidemiologic studies are needed to validate our findings, and also to investigate which pesticide(s)/pesticide components are actually related to HER-2/ neu overexpression, so that proper preventative measures may be adopted. Moreover, despite the lack of an evident relation between pesticides, prognosis, and CD117, this cell marker may nonetheless provide a valuable therapeutic target for select patients with ESSCLC as it does for certain patients with gastrointestinal stromal tumors. Further studies are warranted to investigate that possibility.
| References|| |
|1.||Parkin DM, Pisani P, Ferlay J: Global cancer statistics. CA Cancer J Clin 1999, 49: 33-64. |
|2.||Jemal A, Tiwari RC, Murray T, Ghafoor A, Samuels A, Ward E, Feuer EJ, Thun MJ: American Cancer Society. Cancer statistics, 2004. CA Cancer J Clin 2004, 54: 8-29. |
|3.||Boring CC, Squires TS, Tong T, Montgomery S: Cancer statistics, 1994. CA Cancer J Clin 1994, 44: 7-26. |
|4.||Hoffman PC, Mauer AM, Vokes EE: Lung Cancer. Lancet 2000, 355: 479-5. |
|5.||Chute JP, Venzon DJ, Hankins L, Okunieff P, Frame JN, Ihde DC, Johnson BE: Outcome of patients with small-cell lung cancer during 20 years of clinical research at the US National Cancer Institute. Mayo Clin Proc 1997, 72: 901-912. |
|6.||Potti A, Willardson J, Forseen C, Ganti AK, Hebert B, Levitt R, Mehdi SA: Predictive role of HER-2/neu overexpression and clinical features at initial presentation in patients with extensive stage small cell lung carcinoma. Lung Cancer 2002, 36: 257-61. |
|7.||Micke P, Hengstler JG, Ros R, Bittinger F, Metz T, Gebhard S, Beeh KM, Oesch F, Buhl R: c-erbB-2 expression in small cell lung cancer is associated with poor response. Int J Cancer 2001, 92: 474-9. |
|8.||Schneider PM, Hung MC, Chiocca SM, Manning J, Zhao XY, Fang K, Roth JA: Differential expression of the c-erbB-2 gene in human small cell and non-small cell lung cancer. Cancer Res 1989, 49: 4968-71. |
|9.||Bunn PA Jr, Helfrich B, Soriano AF, Franklin WA, Varella-Garcia M, Hirsch FR, Baron A, Zeng C, Chan DC: Expression of Her-2/neu in human lung cancer cell lines by immunohistochemistry and fluorescence in situ hybridization and its relationship to in vitro cytotoxicity by trastuzumab and chemotherapeutic agents. Clin Cancer Res 2001, 7: 3239-50. |
|10.||Potti A, Moazzam N, Ramar K, Hanekom DS, Kargas S, Koch M: CD117 (c-kit) overexpression in patients with extensive-stage small-cell lung carcinoma. Ann Oncol 2003, 14: 894-897. |
|11.||Yarden Y, Kuang WJ, Yang-Feng T, Coussens L, Munemitsu S, Dull TJ, Chen E, Schlessinger J, Francke U, Ullrich A: Human proto-oncogene c-Kit: a new cell surface receptor tyrosine kinase for an unidentified ligand. EMBO J 1987, 6: 3341-3351. |
|12.||Natali PG, Nicotra MR, Sures I, Santoro E, Bigotti A, Ullrich A: Expression of c-kit receptor in normal and transformed human nonlymphoid tissues. Cancer Res 1992, 52: 6139-6143. |
|13.||Sorrentino V, Giorgi M, Geremia R, Besmer P, Rossi P: Expression of c-kit proto-oncogene in the murine male germ cells. Oncogene 1991, 6: 149-151. |
|14.||Pietsch T, Nicotra MR, Fraioli R, Wolf HK, Mottolese M, Natali PG: Expression of the c-Kit receptor and its ligand SCF in non-small cell lung carcinomas. Int J Cancer 1998, 75: 171-5. |
|15.||Ikeda H, Kanakura Y, Tamaki T, Kuriu A, Kitayama H, Ishikawa J, Kanayama Y, Yonezawa T, Tarui S, Griffin JD: Expression and functional role of the proto-oncogene c-kit in acute myeloblastic leukemia cells. Blood 1991, 78: 2962-8. |
|16.||Clarke LE, Demetri GD, Leitzel K, Ali SM, Harvey HA, Kitoh T, Lipton A: Soluble c-kit in the serum of patients with gastrointestinal stromal tumors (GISTs). Proc Am Soc 2002, 21: 436a. |
|17.||Barrios C, Kappes D, Ritt C, Medaglia F, Marques B, Gaiger AM: Clinical correlation of c-kit expression in small cell lung cancer (SCLC). Proc Am Soc Clin Oncol 2002, 21: 302b. |
|18.||Demetri GD: Targeting C-kit mutations in solid tumors: scientific rationale and novel therapeutic options. Semin Oncol 2001, 28: 19-26. |
|19.||Farrow A, Jacobs A, West RR: Myelodysplasia, chemical exposure, and other environmental factors. Leukemia 1989, 3: 33-5. |
|20.||Brown LM, Blair A, Gibson R, Everett GD, Cantor KP, Schuman LM, Burmeister LF, Van Lier SF, Dick F: Pesticide exposures and other agricultural risk factors for leukemia among men in Iowa and Minnesota. Cancer Res 1990, 50: 6585-91. |
|21.||Zahm SH, Blair A: Pesticides and non-Hodgkin's lymphoma. Cancer Res 1992, 52: 5485s-88s. |
|22.||Jimenez RE, Wallis T, Tabasczka P, Visscher DW: Determination of HER-2/ neu status in breast carcinoma: comparative analysis of immunohistochemistry and fluorescent in situ hybridization. Mod Pathol 2000, 13: 37-45. |
|23.||Buehler H, Bangemann N, Evers K, Becker C, Schaller G: Effective HER-2/ neu diagnosis in breast cancer by a combination of immunochemistry and FISH. Proc Amer Soc Clin Oncol 2000, 19: 76a. |
|24.||Mass RD, Sanders C, Charlene K, Johnson L, Everett T, Anderson S: The concordance between the clinical trials assay (CTA) and fluorescence in situ hybridization (FISH) in the Herceptin pivotal trials. Proc Amer Soc Clin Oncol 2000, 19: 75a. |
|25.||Kaplan EL, Meier P: Nonparametric estimation from incomplete observations. J Am Stat Assoc 1958, 53: 457-81. |
|26.||McCann AH, Dervan PA, O'Regan M, Codd MB, Gullick WJ, Tobin BM, Carney DN: Prognostic significance of c-erbB-2 and estrogen receptor status in human breast cancer. Cancer Res 1991, 51: 3296-303. |
|27.||Weiner DB, Nordberg J, Robinson R, Nowell PC, Gazdar A, Greene MI, Williams WV, Cohen JA, Kern JA: Expression of neu gene-encoded protein (P185neu) in human non-small cell carcinomas of the lung. Cancer Res 1990, 50: 421-5. |
|28.||Zhang X, Silva E, Greshenson D, Hung MC: Amplification and rearrangement of c- erb B proto-oncogenes in cancer of human female genital tract. Oncogene 1989, 4: 985-9. |
|29.||Yokota J, Yamamoto T, Miyajima N, Toyoshima K, Nomura N, Sakamoto H, Yoshida T, Terada M, Sugimura T: Genetic alterations of the c- erb B-2 oncogene occur frequently in tubular adenocarcinoma of the stomach and are often accompanied by amplification of the v-erbA homologue. Oncogene 1988, 2: 283-7. |
|30.||Dugan MC, Dergham ST, Kucway R, Singh K, Biernat L, Du W, Vaitkevicius VK, Crissman JD, Sarkar FH: HER-2/ neu expression in pancreatic adenocarcinoma: Relation to tumor differentiation and survival. Pancreas 1997, 14: 229-36. |
|31.||Kapitanovic S, Radosevic S, Kapitanovic M, Andelinovic S, Ferencic Z, Tavassoli M, Primorac D, Sonicki Z, Spaventi S, Pavelic K, Spaventi R: The expression of p185 (HER-2/ neu ) correlates with the stage of disease and survival in colorectal cancer. Gastroenterology 1997, 112: 1103-13. |
|32.||Riben MW, Malfetano JH, Nazeer T, Muraca PJ, Ambros RA, Ross JS: Identification of HER-2/ neu oncogene amplification by fluorescence in situ hybridization in stage I endometrial carcinoma. Mod Pathol 1997, 10: 823-31. |
|33.||Costa MJ, Walls J, Trelford JD: C- erb B-2 oncoprotein over-expression in uterine cervix carcinoma with glandular differentiation. A frequent event but not an independent prognostic marker because it occurs late in the disease. Am J Clin Pathol 1995, 104: 634-42. |
|34.||Cobleigh MA, Vogel CL, Tripathy D, Robert NJ, Scholl S, Fehrenbacher L, Wolter JM, Paton V, Shak S, Lieberman G, Slamon DJ: Multinational study of the efficacy and safety of humanized anti-HER2 monoclonal antibody in women who have HER2-overexpressing metastatic breast cancer that has progressed after chemotherapy for metastatic disease. J Clin Oncol 1999, 17: 2639-48. |
|35.||Savage DG, Antman KH: Imatinib Mesylate - A New Oral Targeted Therapy. N Engl J Med 2002, 346: 683-93. |
|36.||Dich J, Zahm SH, Hanberg A, Adami HO: Pesticides and cancer. Cancer Causes Control 1997, 8: 420-43. |
|37.||Wicklund KG, Daling JR, Allard J, Weiss NS: Respiratory cancer among orchardists in Washington State, 1968 to 1980. J Occup Med 1988, 30: 561-4. |
|38.||McDuffie HH, Klaassen DJ, Dosman JA: Is pesticide use related to the risk of primary lung cancer in Saskatchewan? J Occup Med 1990, 32: 996-1002. |
|39.||Blair A, Grauman DJ, Lubin JH, Fraumeni JF Jr: Lung cancer and other causes of death among licensed pesticide applicators. J Natl Cancer Inst 1983, 71: 31-7. |
|40.||De Stefani E, Kogevinas M, Boffetta P, Ronco A, Mendilaharsu M: Occupation and the risk of lung cancer in Uruguay. Scand J Work Environ Health 1996, 22: 346-52. |
|41.||Becher H, Flesch-Janys D, Kauppinen T, Kogevinas M, Steindorf K, Manz A, Wahrendorf J: Cancer mortality in German male workers exposed to phenoxy herbicides and dioxins. Cancer Causes Control 1996, 7: 312-21. |
|42.||Pesatori AC, Sontag JM, Lubin JH, Consonni D, Blair A: Cohort mortality and nested case-control study of lung cancer among structural pest control workers in Florida (United States). Cancer Causes Control 1994, 5: 310-8. |
|43.||Tessier DM, Matsumura F: Increased ErbB-2 tyrosine kinase activity, MAPK phosphorylation, and cell proliferation in the prostate cancer cell line LNCaP following treatment by select pesticides. Toxicol Sci 2001, 60: 38-43. |
|44.||Enan E, Matsumura F: Activation of c-Neu tyrosine kinase by o,p'-DDT and beta-HCH in cell-free and intact cell preparations from MCF-7 human breast cancer cells. J Biochem Mol Toxicol 1998, 12: 83-92. |
|45.||Potti A, Ganti AK, Sholes K, Langness E, Koka V, Horvarth L, Koch M: Effect of pesticide exposure on HER-2/neu overexpression seen in patients with extensive stage small cell lung carcinoma. Clin Cancer Res 2003, 9: 4872-6. |
|46.||Sekido Y, Obata Y, Ueda R, Hida T, Suyama M, Shimokata K, Ariyoshi Y, Takahashi T: Preferential expression of c-kit proto-oncogene transcripts in small cell lung cancer. Cancer Res 1991, 51: 2416-9. |
|47.||Hibi K, Takahashi T, Sekido Y, Ueda R, Hida T, Ariyoshi Y, Takagi H, Takahashi T: Coexpression of the stem cell factor and the c-kit genes in small cell-lung cancer. Oncogene 1991, 6: 2291-6. |
|48.||Gazdar AF: The molecular and cellular basis of human lung cancer. Anticancer Res 1994, 14: 261-7. |
|49.||Hornick JL, Fletcher CD: Immunohistochemical staining for KIT (CD117) in soft tissue sarcomas is very limited in distribution. Am J Clin Pathol 2002, 117: 188-193. |
|50.||Fletcher CD, Fletcher JA: Testing for KIT (CD117) in gastrointestinal stromal tumors: another Hercep test? Am J Clin Pathol 2002, 118: 163-164. |
|51.||Coughlin SS: Recall bias in epidemiologic studies. J Clin Epidemiol 1990, 43: 87-91. |
|52.||Teschke K, Smith JC, Olshan AF: Evidence of recall bias in volunteered vs. prompted responses about occupational exposures. Am J Ind Med 2000, 38: 385-8. |
|This article has been cited by|
||Overexpression of HER-2/neu in patients with colorectal cancer (CC) and colorectal adenomas (CP)
| ||Pazurek, M., Smolarz, B., Romanowicz-Makowska, H., Kulig, A., Małecka-Panas, E. |
| ||Clinical and Experimental Medical Letters. 2009; 50(3): 179-182 |
||Cancer stem cells: The lessons from pre-cancerous stem cells: Stem Cells Review Series
| ||Gao, J.-X. |
| ||Journal of Cellular and Molecular Medicine. 2008; 12(1): 67-96 |
||Targeted therapy for small cell lung cancer
| ||Ganti, A.K., Panwalkar, A.W. |
| ||Targeted Oncology. 2007; 2(2): 89-97 |
||Precancerous stem cells have the potential for both benign and malignant differentiation
| ||Chen, L., Shen, R., Ye, Y., Pu, X.-A., Liu, X., Duan, W., Wen, J., (...), Gao, J.-X. |
| ||PLoS ONE. 2007; 2(3): Art e293 |
||Treatment options for relapsed small-cell lung cancer
| ||Azim Jr., H.A., Ganti, A.K. |
| ||Anti-Cancer Drugs. 2007; 18(3): 255-261 |
||Limited-stage small-cell lung cancer: Therapeutic options
| ||Ganti, A.K., Zhen, W., Kessinger, A. |
| ||ONCOLOGY. 2007; 21(3): 303-312 |
||Stem Cells Review Series: Cancer stem cells: the lessons from pre-cancerous stem cells
| ||Jian-Xin Gao |
| ||Journal of Cellular and Molecular Medicine. 2007; 12(1): 67 |
|[VIEW] | [DOI]|
||Targeted therapy for small cell lung cancer
| ||Apar Kishor Ganti,Amit W. Panwalkar |
| ||Targeted Oncology. 2007; 2(2): 89 |
|[Pubmed] | [DOI]|
||Treatment options for relapsed small-cell lung cancer
| ||Hatem A. Azim,Apar Kishor Ganti |
| ||Anti-Cancer Drugs. 2007; 18(3): 255 |
|[Pubmed] | [DOI]|
||Analysis of c-kit expression in small cell lung cancer: Prevalence and prognostic implications
| ||Carlos Camps,Rafael Sirera,Roy M. Bremnes,Javier Garde,María José Safont,Ana Blasco,Alfonso Berrocal,José Javier Sánchez,Consuelo Calabuig,Miguel Martorell |
| ||Lung Cancer. 2006; 52(3): 343 |
|[Pubmed] | [DOI]|
||Analysis of c-kit expression in small cell lung cancer: Prevalence and prognostic implications
| ||Camps, C., Sirera, R., Bremnes, R.M., Garde, J., Safont, M.J., Blasco, A., Berrocal, A., (...), Martorell, M. |
| ||Lung Cancer. 2006; 52(3): 343-347 |